Inoculation responses of perennial forage legumes grown in fresh hill‐land ultisols as affected by soil acidity‐related factors

A growth chamber experiment was initiated with two field moist, marginal and acidic (pH 5.1–5.2) soils of the Lily series (Typic Hapludults) in order to determine the need for improved legume‐rhizobia symbioses for forage species of current, or potential, use in the renovation of Appalachian hill‐land pastures. One soil was from an abandoned pasture having broomsedge (Andropogon virginicus L.) as the predominant vegetation, whereas the other was from a minimally‐managed pasture dominated by orchardgrass (Dactylis glomerata L.). Treatments included inoculation (or no inoculation) and the addition of aluminum, nil, or lime to provide a range of soil acidities. Both soils contained effective populations of naturalized rhizobia for white clover (Trifolium repens L.) and red clover (Trifolium pratense L.), but low and/or ineffective naturalized populations of rhizobia for alfalfa (Medicago sativa L.), birdsfoot trefoil (Lotus corniculatus L.), bigflower vetch (Vicia grandiflora Scop.), and flatpea (Lathyrus sylvestris L.). Seed inoculation, by lime‐pelleting, was highly beneficial in establishing effective symbioses for all these latter species. The addition of low levels of aluminum or lime (1.5 and 2.0 cmol/kg soil, respectively) had little effect on any of the symbioses, with the exception of those for alfalfa. Thus, an improved legume rhizobia symbiosis would not seem to be a prerequisite for renovating pastures established on chemically similar ultisols with the forage legume species examined in this study, especially if the pasture has at least some history of management.     

Tolerance of forage legumes to lime‐stabilized sludge

Abstract

Lime‐stabilized sludge (LSS) from dairy processing waste‐water treatment plants is a desirable product for land application. The material contains lime, which neutralizes soil acidity, and P, which is useful as a plant nutrient. The fineness of the lime and the solubility of P make LSS especially desirable in establishing forage legumes. This greenhouse study had two objectives: to determine a reasonable quantity of LSS for establishing forage legumes such as alfalfa (Medicago sativa L.) and red clover (Trifolium pratense L.) and to prevent adverse effects on seedlings. Sludge was applied at 0, 2.5, 5.0, 7.5 g kg^‐1 to an acid, low P soil in pots, and alfalfa and red clover seeds were sown. All treatments received 123 μg g^‐1 potassium as KCl. A completely randomized design with four replications was used. Each species was handled as a separate study. Dry matter production was measured at one‐tenth bloom stage. Plant samples were analyzed for P, K, Ca, and Mg content. Soil samples taken at the end of the study were analyzed for pH, organic matter, Bray P, K, Ca, Mg, exchangeable Al, EC, and CEC. The higher quantities of LSS (7.5 g kg^‐1 for alfalfa and 5.0 g kg^‐1 for red clover) had negative effects on seedling germination and establishment. Lime‐stabilized sludge resulted in an increase in total nutrient uptake of Ca, Mg, K, and P up to 5.0 and 2.5 g kg^‐1 in alfalfa and red clover, respectively. In both species significant dry matter yield increases were obtained with LSS up to 5.0 g kg^‐1; however, 7.5 g kg^‐1 caused a reduction in dry matter yield. Based on these results, applications of LSS at 5.0 for alfalfa and 2.5 g kg^‐1 for red clover had positive effects in seedling establishment, nutrient uptake, and dry matter production. Lime‐stabilized sludge application resulted in significant increases in soil pH, available P, Ca, Mg, EC, and CEC; decreases were seen in neutralizable acidity and exchangeable Al levels in soil. This study indicates that LSS is appropriate for the acidic, low P soils of Southern Missouri for alfalfa and red clover establishment and production, if applied in appropriate quantities.     

Growth of apple seedlings on sludge‐amended soils in the greenhouse

Abstract

Open pollinated ‘York Imperial’ apple (Malus domestica Borkh.) seeds were germinated and grown for a period of 7 months in: (1) sand with complete nutrient solutions added; (2) limed and unlimed soil, (3) limed and unlimed soil amended with two different sewage sludges at rates of 25, 50 or 100 dry kg ha^‐1. A third composted, lime stabilized sludge was added either sieved or non‐sieved (to remove wood chips) at the same rates. The sludge materials used were: (1) a high metal, composted sludge from Baltimore, MD (BALT); (2) a high Cd sewage sludge (CITY) and (3) a low metal, composted sewage sludge from Washington, D.C. (DC).

Germination was unaffected by treatments. After 7 months, the best growth was obtained from the sand plus nutrient solution media. Two of the three sludge materials increased seedling growth over that of the soil, either limed or unlimed. The BALT compost treated soils produced the lowest growth, particularly when unlimed. Elevated tissue metal levels indicated that Mn, Zn, Cu and Ni were the probable causes of reduced growth noted from the BALT compost treatment. The use of soil with or without low metal sludges as media for early apple seedling growth when compared to standard sand culture is not recommended.     

Enzyme activities in Appalachian soils: 3. Pyro‐phosphatase

Abstract

The pyrophosphatase (PPi) enzyme catalyzes the hydrolysis of pyrophosphate to orthophosphate. The PPi activity was determined in 14 hill‐land soils of the Appalachian Region. The top two horizons from each soil were sampled and stored in a field‐moist state at 4°C (4°C) and in an air‐dry (AD) state prior to determination of PPi activity. Each soil type had its own level of PPi activity. The mean PPi activities of surface and subsurface horizons stored at 4°C were 1.3 and 1.7 times higher than those of AD samples. The average PPi activities of surface horizons were 6.2 and 4.6 times higher than subsurface horizons stored at AD and 4°C. respectively. The PPi activities were positively correlated with organic C, N, forms of S and P. exchangeable cations, original moisture by weight and volume, and percent air‐filled porosity. In both surface and subsurface horizons, significant positive correlationships were observed between PPi activities and Mn content, indicating the need for Mn in the activation of PPi. High PPi activities in surface horizons might induce a greater rate of hydrolysis of applied pyrophosphate (polyphosphate) fertilizers to orthophosphate and lead to undesirable fixation of P in acid soils.     

Potassium‐sparing effect of calcium in perennial ryegrass

Perennial ryegrass in soil culture was treated with different rates of potassium fertilizer and calcium carbonate, to determine if calcium could substitute for potassium in plant shoot tissue without interfering with dry matter production. By increasing the concentration of calcium in plant shoots to approximately 0.8% in the dry matter, the critical potassium concentration was decreased to 0.6%. This critical potassium concentration was probably the minimum concentration necessary to maintain essential potassium‐specific metabolic processes in perennial ryegrass shoots.     

Fixation of potassium in some soils of the sub‐humid zone of Nigeria

Abstract

Studies of potassium (K) fixation in the soil were conducted by evaluating the effect of applied K on the extractability of K with time. A series of five K‐sorption treatment solutions, 0.11, 0.22, 0.45, 0.90, and 1.80 cmol/kg were prepared and applied as potassium chloride (KCl) to three sets of soils. The first set of soil samples was extracted with one normal ammonium acetate (1N NH₄OAc) extractant for K after one day of incubation. The second and third sets were extracted with the same extractant after seven and 42 days of incubation, respectively. The amount of K fixed was determined. Correlation between applied K and K fixed was carried out. The mean proportion of K fixed ranged from 0 in soils from Kurmin Biri to 55% in soils from Funafuna upon addition of 0.11 cmol K/kg. While fixation increased with increase in the concentration of added K, there was no linear relationship between the proportion of K fixed and the amount added at higher incubation periods. Potassium recovered also increased with added K in all the incubation periods with the 42‐day period having the highest amount of K recovered. Potassium added was highly correlated (P<0.01) with K fixed during all the incubation periods.     

Grasses and legumes facilitate phytoremediation of metalliferous soils in the vicinity of an abandoned chromite–asbestos mine

Purpose

The present study was carried out in Roro region, Chaibasa, Jharkhand, India, to assess the impact of chromite–asbestos mine waste (CMW) on a nearby agroecosystem. The role of metal-accumulating grass–legume association in facilitating phytoremediation was investigated.

Materials and methods

Soil and plant samples were collected from (i) chromite–asbestos mine waste (CMW) with Cynodon dactylon, Sorghastrum nutans, and Acacia concinna; (ii) contaminated agricultural soil-1 (CAS1) from a foothill with Cajanus cajan; (iii) contaminated agricultural soil-2 (CAS2) distantly located from the hill, cultivated with Oryza sativa and Zea mays; and (iv) unpolluted control soil (CS). Total metal concentrations were quantified in both soils and plants by digesting the samples using HNO₃, HF, HClO₄ (5:1:1; v/v/v), and HNO₃ and HClO₄ (5:1; v/v), respectively, and analyzed under flame atomic absorption spectrophotometry. Metal grouping and site grouping cluster analysis was executed to group the metals and sampling sites. Translocation factor (TF) and bioconcentration factor (BCF) were calculated to determine the phytoremediation efficiency of grasses and legumes.

Results and discussion

Results indicate that total metal concentrations in the CMW were in the order of Cr?>?Ni?>?Mn?>?Cu?>?Pb?>?Co?>?Zn?>?Cd. High concentrations of Cr (1983 mg kg^?1) and Ni (1293 mg kg^?1) with a very strong contamination factor were found in the CAS, which exceeds the soil threshold limits. Further, metal and site grouping cluster analysis also revealed that Cr and Ni were closely linked with each other and the CMW was the main source of contamination. Among all the metals, Cr and Ni were mainly accumulated in grasses (C. dactylon and S. nutans) and legumes (A. concinna and C. cajan) as compared to cereals (Z. mays and O. sativa). The TF of Cr was >1 for grasses. Except for Zn, the BCF for all the metals were <1 in roots and shoots of all the plants and cereals.

Conclusions

The present study revealed that abandoned CMW is the source of contamination for agriculture lands. Phytoremediation relies on suitable plants with metal-scavenging properties. Grass–legume cover (C. dactylon, S. nutans, A. concinna, and C. cajan) has the ability to accumulate metals and act as a potential barrier for metal transport, which facilitate the phytoremediation of the CMW. Possibilities for enhancing the barrier function of the grass–legume cover need to be explored with other low-cost agronomic amendments and the role of rhizospheric organisms.

     

Obtaining empirical equations for the process of formation‐decomposition of FeEDDHA in soils

Abstract

This work is included in a wide field of research on the dynamics of synthetic chelates in calcareous soils of South‐East of Spain. Through the application of Freundlich isotherm to the process of formation‐decomposition of chelate FeEDDHA, equations of type: C_s = A . tⁿ . C^m _o are obtained, where A, n and m, are ctes., C_s, the concentration of iron chelated added to the soil, and t, interaction time of chelate with the soil. In this way we can predict the rhythm of the solution process of Fe in calcareous soils.     

Colorimetric determination of phosphorus in citrate‐bicarbonate‐dithionite extracts of soils

Abstract

Existing colorimetric methods for determining phosphorus (P) in citrate‐bicarbonate‐dithionite (CBD) extracts from soils and sediments require pretreatments of extracts prior to the determination of the element. A method is proposed for the determination of P in CBD extracts without any chemical treatments. Maintaining the citrate concentration below 2.4 mM, maximum and stable absorbance develops in P‐Mo‐Sb system within one hour and remains stable for 20 hours. An evaluation of potential interference was made by adding varying amounts of P to CBD extracts over a range of extractable iron (Fe) and aluminum (Al) levels. Near 100 percent recovery of the added P suggests the applicability of the method to soils and sediments. Major advantages of the method are speed, simplicity, reliability and stability of the colored complex.     

Quantity‐intensity parameters of potassium in relation to uptake by guinea‐corn in representative soils of the ecological zones of Nigeria

Abstract

Quantity‐intensity (Q‐I) relation studies were often used to supplement information obtained from conventional soil tests for the estimation of potassium (K) needs of crops. With a view to ascertaining the reliability of the Q‐I relation parameters for comprehensive characterization of K dynamics in typical Nigerian soils, K values derived from Q‐I isotherms were related to neutral normal ammonium acetate (1 N NH₄OAc, pH 7.0) (exchangeable) K, other soil K forms [non‐exchangeable (K_ne), exchange (K_e), mineral K (K _m ), and solution K (K_s)] and the K uptake by Guinea‐corn (Sorghum bicolor, var. LS 187) subjected to weekly cuts in Neubauer cultivation vessels. Most of the soil K (about 98%) was in the form of soil minerals while less than 1% was plant available whereas about 1% was trapped within the interlattice layers of the clay minerals (as fixed K or K_ne). Mineral K (K_m) content was closely related to total K (K_t), but not to the other forms, K_ne, K_e, and K_s. A close relationship was noted between the two components of labile K (K_e and K_s). Except for % K saturation, the relationships between the K measurements with plant response were poor. The results of these investigations clearly demonstrate that the Q‐I relation could not adequately characterize the K dynamics of these tropical soils.     

Single‐Hole Soil Sampling for Nitrogen in the Potato Hill

Abstract

The nitrate distribution in the soil profile varies with fertilization and tillage practices in potato (Solanum tuberosum L.) production. Band‐applied fertilizers localized near the seed at planting must diffuse through the bulk soil during the growing season. The hilling operation transforms soil surface into an undulating field landscape and redistributes the split‐applied nitrogen fertilizers between the hill and the interrow. The soil sampling procedure during the growing season thus becomes extremely tedious when searching to quantify nitrate accumulation in the entire soil volume. The objective of this study was to assess seasonal nitrate accumulation in a soil volume from a single boring in the potato hill. An intensive sampling was conducted at four places in the 0‐ to 50‐cm profile in potato fields receiving three rates of split-applied nitrogen (N) before hilling. Treatment and time effects provided a large range of nitrate concentrations throughout the soil profile. Nitrate content increased with N fertilization and organic‐matter mineralization and decreased as a result of plant uptake and nitrate leaching. Averaged across the season, nitrate accumulation in the 0‐ to 50‐cm profile represented 78% of that accumulated in the center of the hill on a per ha basis (r²=0.90). A single boring in the center of the hill considerably reduced sampling time and cost and provided a fair estimate of seasonal nitrate accumulation in the 0‐ to 50‐cm soil profile.     

Effect of temperature on EDTA‐extractable copper in soils

Abstract

Two contrasting soils were extracted with 0.05 M EDTA in 1 M CH₃ COONH₄ at pH 6, before and after incubation for 4 weeks at constant (10, 20 or 30°C) or fluctuating (10/30, mean 20°C) temperatures. Less copper was extracted from soils which were incubated at fluctuating temperature than from those maintained at a constant 20 C. Where incubation temperature was constant, extractable copper increased or decreased with increasing temperature depending on the soil and how it was treated. Recovery of added copper was low initially but increased during the incubation. Maximum recovery was associated with low incubation temperature in one soil, but high temperature in the other. The amounts of copper extracted were slightly increased by γ‐irradiation of the soils. Extractable copper was also increased by increasing the temperature at which the extraction was performed.     

Determination of total cadmium in calcareous soils by extraction using aliquat‐336 and 3‐heptan‐one after aqua regia digestion

Abstract

Measurement of total soil cadmium (Cd) is difficult due to calcium (Ca) and other chemicals which cause high background absorbance when trace levels of Cd are to be determined. When soil Cd is low, even use of deuterium background correction with flame atomic absorption spectroscopy (AAS) cannot provide accurate Cd results. Use of furnace atomic absorption with method of standard additions can circumvent these interferences, but the cost and time required are substantial. We desired a more rapid, convenient, and reliable alternative to extraction using dithizone and back‐extraction into acid, or to ammonium pyrollidinedithiocarbamate (APDC) which does not require close pH adjustment nor have many sources of potantial contamination. We evaluated analysis of these complex soil extracts with the method of Viets (1978) which extracts metals from 1N acid solutions using Aliquat‐336 in methylisobutyl‐ketone (MIBK). We tested the use of the less toxic and less water soluble 3‐heptanone as an organic solvent alternative to MIBK which can be directly analyzed by flame atomic absorption. A series of extraction experiments were conducted to determine if Cd was extracted from standard solutions and from total metal digests of calcareous soils into an Aliquat‐336/3‐heptanone solution, and under what conditions extraction was optimum. In the optimum method, Cd was extracted from aqua regia soil digests by 10% Aliquat‐336 in 3‐heptanone without addition of ascorbic acid or potassium iodide (KI) used by Viets. Excellent recovery of Cd was obtained for both standard reference soils and low Cd highly calcareous soils from North Dakota and Minnesota. Addition of ascorbic acid and KI did not increase the efficiency of extraction indicating that the extraction system used was free of ferric‐iron [Fe(III)] interference. The ion‐association complex of Cd remained stable for at least 24 hr after extraction, providing a very convenient method to analyze low levels of total Cd in soils and other geologic materials.     

Sulfur status of volcanic ash‐derived soils in Hawaii

Abstract

Several rainwater samples and 14 profiles of Hawaii's volcanic ash‐derived soils were analyzed for sulfur (S). Atmospheric deposition was an important S source at the coast (24 kg S/ha), but its contribution decreased with increasing distance from the sea (1 kg S/ha at 24‐km inland). The S concentration of rainwaters also decreased linearly with increasing rainfall.

Several thousand mg SO₄‐S/kg can be extracted from many volcanic ash‐derived soils of Hawaii, and it was often required at least four extractions [0.04 M Ca(H₂PO₄)₂, 1:10 soil to solution ratio] to completely desorb this SO₄. There was a close association of high SO₄ retention with high rainfall. This might have resulted from (1) the development of a solid phase with high SO₄ retention under intense weathering conditions, (2) more total SO₄ received by the soils from atmospheric deposition, and (3) past fertilization of sugarcane grown in high rainfall areas.

Low concentrations of soil solution SO₄‐S in relation to large amounts of P‐extractable SO₄ suggest that a S bearing mineral, such as basaluminite, may be controlling soil‐solution SO₄. Furthermore, SO₄ adsorption isotherms of these volcanic soils generally show a bi‐phasic property, and suggest that 40 to 80 mg SO₄‐S/kg is required to maintain 3 ‐ 6 mg SO₄‐S/L in the soil solution, a concentration range considered adequate for the growth of most crops.     

Phosphorus‐sorption characteristics of intensely weathered soils in south‐central kentucky

Abstract

Studies were conducted to investigate phosphorus (P)‐sorption characteristics of some intensely weathered soils in south‐central Kentucky. Phosphorus adsorption characteristics reflected the chemical and mineralogical properties of the soils studied. All adsorption data were adequately described by first order kinetic reactions which implied that the soils have uniform surfaces for P sorption. In spite of the limitations of the Langmuir equation, its usefulness in summarizing data into one adsorption maximum value was demonstrated by nearly identical adsorption maxima estimated by three linear transformations of the equation and small deviations from the observed maxima. Variations in adsorption maxima between surface and subsoils and among soils were best correlated with extractable aluminum (Al) (r = 0.93, p<0.01) and crystalline iron (Fe) oxy‐hydroxides (r = 0.97, p<0.01). Clay content was also highly correlated with P sorption (r = 0.97, p <0.01) as well as with extractable Al (r = 0.83, p<0.05) and crystalline Fe oxides (r = 0.92, p<0.01) suggesting that its contribution may have been through its association with these soil components. In contrast, organic matter had a negative association with P sorption (r = ‐0.83, p<0.05). The results indicate higher P sorption in subsoil than in surface horizons, controlled mainly by extractable Al and crystalline Fe oxyhydroxides.     

A new soil test method for the determination of plant‐available cadmium in soils

Abstract

A new soil test procedure using 1M NH₄Cl was developed for the extraction of plant‐available cadmium (Cd) from soils. Five grams of soil is weighed into a 50‐mL polyethylene vial to which 30 mL of 1M NH₄Cl solution is added. The soil suspension is then shaken on a horizontal shaker for 16 h at 25°C at 180 cycles per min. The suspension is then centrifuged at 2,500g for 5 min and the supernatant filtered through a 0.45 μm nitrocellulose filter under vacuum. Cadmium in the extract is then determined at 228.8 nm on a graphite furnace equipped atomic absorption spectrophotometer. A highly significant correlation was observed between the natural logarithm (In) of 1M NH₄Cl‐extractable Cd in soils and the Cd content in the grain of durum wheat (Triticum turgidum var. durutn L.) grown on the same soils (r = 0.974, p = 3.8 x 10^‐7). In comparison with several commonly used extradants, such as ABDTPA, CaCl₂, NH₄OAc, and NH₄NO₃, the 1M NH₄Cl‐extracted Cd from soils was found to be a better index of Cd availability.     

Origin of the effect of ph on the saturated hydraulic conductivity of non‐sodic soils

Abstract

The effect of pH on the saturated hydraulic conductivity (K) of repacked columns of two non‐sodic soils (Healaugh and Fagaga soils) was examined. The K value was greater for the Fagaga soil than for the Healaugh soil which is attributed to the difference in the amount of free iron oxides between the soils. The K values reached a maximum when the pH was close to the point of zero net charge (PZNC) (3.7 and 4.8 for the Healaugh and the Fagaga soil, respectively) and decreased on either side of these pH values. The effect of pH on K was related to its effect on surface charge. As the pH of variable‐charge soils approaches the PZNC, the net surface charge decreases resulting in flocculation and maintenance of a high K. Conversely, as the pH deviates from the PZNC, the net surface charge increases, resulting in dispersion and a decrease in K. There was a negative relationship between the amount of dispersed clay and the K values, suggesting that clay dispersion and the resulting clogging of pores decreases K in these soils.     

Reactions of copper sulfate with wetland‐taro soils in Hawaii

Abstract

The environmental impact of copper sulfate (CuSO₄#lb5H₂O) must be evaluated before the chemical can be registered as a pesticide to control the apple snail (Pomacea canaliculata) in Hawaii's wetlands. To help achieve this goal, we investigated the sorption‐desorption reactions of CuSO₄#lb5H₂O with six wetland‐taro soils (Tropaquepts) of Hawaii. Our results indicated that: (i) copper (Cu) was sorbed rapidly: 98.0–99.9% of the added Cu was removed from solution within one hour when the loading rate was less than or equal to 300 mg Cu kg^‐1 [initial Cu concentration = 30.0 mg Cu L^‐1 or 12 kg (ha‐cm)^‐1 as CuSO₄#lb5H₂O which is 10 times the maximum recommended rate of pesticide applications, (ii) Cu sorption increased as soil pH increased from 5.0 to 8.0, and (iii) sorption capacity varied from 210 mg Cu kg^‐1 in a Tropaquept from Kauai Island to 500 mg Cu kg^‐1 in another Tropaquept from Maui Island, after seven days of incubation at soil‐solution pH 6.0 and total solution Cu concentration of 0.10 mg Cu L^‐1, a Cu level deemed toxic to some living organisms. It appears that more Cu was sorbed (less Cu remained in solution) if the soil contained high organic carbon (C) and low indigenous Cu. Also, there was an inverse relationship between Cu sorption and desorption by the soils tested: the more Cu a soil can sorb, the tighter it holds Cu, and the less Cu it releases. Since soil pH increases by 1 to 1.5 units upon flooding and Cu sorption increases with increasing pH, the recommended practice of flooding the soil for at least 48 hours between CuSO₄#lb5H₂O application and crop planting should be followed.     

Behavior of iron‐supplying materials in incubated calcareous soils 1

Two Fe chlorosis‐inducing calcareous soils were incubated for up to 5 months, at room temperature and field capacity, with Fe‐EDDHA, Fe‐DTPA, FeSO₄, an amino acid chelate “Fe‐Metalosate”;, an oxide “Micronized‐Iron”;, and a precipitated Fe‐S compound “Iron‐Sul”;. Other treatments included DTPA chelate alone, elemental S and H₂SO₄ at comparable rates. Both water‐soluble, and DTPA‐extractable Fe fractions were measured periodically from each sample. All water‐soluble sources decreased with time. Soluble Fe was highest after Fe‐EDDHA addition but was not detectable after “Fe‐Metalosate”; and FeSO₄. Acidification to neutralize CaCO₃ significantly increased DTPA‐extractable Fe, which remained high with increasing incubation time. “Micronized‐Iron”; and S had only a slight effect on DTPA‐ extractable Fe. Though Fe‐EDDHA is the most efficient Fe material, pelleted acidified Fe sources, i.e., “Iron‐Sul”;, may be more economical for some crops in the long term.     

On some general regularities of the formation and changes in properties of mn‐fe concretions in soils of humid landscapes

An attempt is made to formulate general regularities of changes in the amount and composition of Mn‐Fe conoretions in soils of humid landscapes, confined to various soil‐forming rocks within the Russian platform. It is concluded, that the intensive formation of concretions is highly conditioned by waterlogging degree of soils and their hydrological regime. The content of concretions is always maximum in gley‐like soils (seldom in gley ones), independing on genesis of parent rocks; the fraction distribution of Mn‐Fe concretions proves to be stable in time; Mn amount is declined with increasing the waterloggiing degree of soils, while the content of Fe becomes increased; the highest accumulation of such microelements as Co, Pb, Cd is observed in concretions, which are rich in Mn. The concretions are characterized by a high amount of X‐ray‐amorphous Fe as well as by a low magnetic susceptibility. The chemical composition of concretions is shown to be preferable for quantitative diagnosis of the water‐logging degree in soils.