Skip to main content

Microbial features of mature and abandoned soils in refractory clay deposits

Abstract

Processes of soil restoration in anthropogenically disturbed soils is an urgent topic in modern ecology and nature management. Being mediator between mineral soil composition and plant vegetation, soil microbial community is important factor of soil restoration processes. Analysis of main soil nutrition components followed by 16S amplicon sequencing are sufficient methods for primary analysis of novel locations. Here is the primary analysis in a novel location in Northwest Europe (Russia). Main nutrition parameters (pH, P, Na and NH4+) and 16S rDNA Illumina amplicons were explored in abandoned soils from sandy pit quarry (2 sites) and refractory clay mining dumps (4 sites).

Microbial communities of mature soils and dumps are variable and different in terms both nutritional and microbial components. pH, N and TOC are strong predictors for microbial composition. Dumps of refractory clays pQ_2 are non-developed soils, highly acidic and form specific microbial community. Differences between dumps and mature soils in both pre-quaternary and quaternary soils are connected with specific bacterial taxa. Those taxa are connected more with plant composition, not the soil properties themselves. The exact changes in microbial community are unique for different soils and areas.

Graphical Abstract

Peer Review reports

Introduction

Novgorod region is located in the west of the European part of the Russia. The diversity of minerals is especially great in the eastern part of the region, which contributes to intensive mining and disruption of the natural environment. Main substances mined in the region are refractory clays, sand and gravel.

Terrestrial ecosystems of industrial and urbanized territories are very different from natural landscapes. The urbanization process leads to a radical disruption of natural ecosystems, while the industrial development of resources, including mining, often ends with the complete destruction of the soil and vegetation cover [1, 2]. Partial transformation or significant disturbance of ecosystems is an urgent problem of modern ecology and nature management, which must be solved also by introducing of ecological management elements. Numerous challenges in environmental management are complicated by increasing of areas, occupied by open cut mines and heaps on the land surfaces [3, 4]. These heaps, exposed to effect of soil forming factors, could be considered as a model of primary soil formation [5]. Such a model serves as informative tool for evaluation of initial soil formation rate, biogenic-abiogenic interactions and restoration ecosystems [6]. At the same time, exposing on the surface of landscape of parent materials, which are unusual for current quaternary cover, result in developing of pedogenesis in complicated geogenic (lithogenic and topographic) conditions; namely, in overcomposed, hyperskeletic or toxic parent materials [7].

Exposure of mineral substrates of pre-quaternary genesis on the surface of quarry dumps and waste heaps leads to the alternative processing of initial soil, since in modern terrestrial ecosystems soil formation occurs mainly on rocks well processed by exogenous processes. Primary soils formed on non-regular rocks are very different from embryozems on quaternary substrates [8]. In this regard, it is interesting to study the morphological organization, chemical properties and microbiological parameters of primary soils and soil-like bodies formed on newly exposed dumps of various material and chemical composition. Morphological and chemical studies of the soils of various quarries were previously carried out [9] in various natural zones.

Microbial community is an important component in soil development processes. There are several studies of the microbiome of disturbed soils using high-throughput sequencing methods [5, 10, 11]. Despite it, this theme is far from generalization. Microbial shifts are unique for soils with different legacy and properties and should be investigated in multiple sources and processes. This research is dedicated to the exploration of microbial shifts in processes of soil restoration in a relatively novel location – abandoned refractory clays’ deposits in Northwest Europe.

Materials and methods

Four sites were selected in the area of abandoned extraction of refractory clays (pre-quaternary soils pQ_1 – pQ_3 and pQ_R), and two sites in the area of abandoned extraction of sandy deposits (quaternary deposits Q_1 and Q_R): both locations were abandoned 20–30 years ago. The soils around of both the refractory clay deposit and the sand pit are represented by zonal variants (Albeluvisols, or retisols, according WRB 2015). In the first site the zonal soil is sod-podzolic light loamy soil on red-brown non-carbonate moraine sediments (Retisol Loamic). Refractory clay mining dumps are formed only by dumps of moraine material; no signs of horizon formation have been revealed on toxic soils or waste heaps (Primary soil or Entisols). The sandy quarry dumps belong to the embryonic soil (Entisol), characterized by a developed gray-humus horizon; however, signs of podsolization are not developed due to the short time of soil formation. Chemical parameters of soils and dump substrates are given in the Supplementary Table 1.

Samples were collected in 26th of August, 2020 in 3 replicates from each spot. Description of sampling sites and their global location are in Table 1 and Fig. 1 respectively. Samples for microbiological analysis were collected from topsoil (in Table 1 the horizon of sampling is marked by asterisk), frozen, transported and stored at -20 °C. Samples for agrochemical analysis were collected in zip-lock plastic bags and stored at + 4 °C. For all samples main nutrition parameters were determined – pH [12], available phosphorus [13] and potassium, ammonium and nitrate nitrogen [14]. Total organic carbon (TOC) was determined using a CHN analyzer Leco CHN-628 (Leco Corporation, USA). Soil routine analyses were performed in accordance with Kimeklis et al., 2021 [5].

Table 1 Sample description
Fig. 1
figure 1

Global location of sampling areas

DNA was isolated using the MN FastDNA Spin Kit (MN, Germany) using a Precellus 24 homogenizer (Bertin, USA). The quality control of the isolation was carried out by PCR and agarose gel electrophoresis. Due well-developed methods of taxonomical annotation and relatively representative sequencing, the v4 variable region (f515/r806) of 16S rDNA gene was selected for future analysis. Sequencing of the variable region was performed on the Illumina MiSEQ sequencer using primers f515 (GTGCCAGCMGCCGCGGTAA) and r806 (GGACTACVSGGGTATCTAAT) [15]. The datasets generated and analyzed during the current study are available in the SRA repository, https://www.ncbi.nlm.nih.gov/sra/PRJNA705583

The general processing of sequences was carried out on the dada2 (v1.14.1) package [16]. Reads were filtered by length (240 bp for forwards and 180 for reverse) and expected errors’ rate (maxEE = 2) no N were allowed. Reads were paired by “consensus” method, and annotate using Bayesian Naive classifier using SILVA 134 database as the training set [17]. The main diversity analysis of the results was carried out using the phyloseq (v1.30.0) package [18] in R (v3.6.3). Differential abundance of taxa in pairwise comparisons was estimated using DESeq2 (v1.26.0) [19]. Difference in abundances (marking ASV as “variable”) was determined by two thresholds (baseMean >  = 10 and log2FoldChange >  = 2) and p-adj < 0.05. CCA analysis performed in vegan package (2.5–6) [20].

Results

Nutritional properties of soils in common are typical for regional soils (Supplementary Table 1). Mature soils on moraine substrates are characterized by a neutral pH, while the background soil is slightly acidic. Spoil heaps are characterized by strongly acidic reaction (in this case, due to the presence of pyrite, oxidized to sulfuric acid and potassium sulfate). For both sandy soils acidic reaction of the environment is close to neutral. Low carbon and nitrogen content are typical for waste heaps and toxic rocks. In all explored samples most common form of nitrogen is ammonium. This indicates an active transformation of nitrogen-containing organic substances, which does not come into nitrification, which is reasonable for young soil formations. In substrates of quaternary origin there are more available phosphorus and potassium. (excluding toxic spoil heaps). Thus, the studied substrates are different in their initial physicochemical parameters and regimes of nutrients.

The total number of sequences after processing was 1 461 079 in 13 327 ASVs (Amplicon Sequence Variants). According results of pre-processing, the number of reads per sample for pQ_3 samples did not exceed 1500, and these samples were not used for further analysis. Alongside Bacteria, there were Archaea-attributed ASVs, but their abundance was less than 0.1%.

Results of the analysis of alpha diversity are in Fig. 2. According to ANOVA, values of all indices are different in all groups (Observed: F = 85.6, p < 0.01, df1 = 4, df2 = 50; Simpson: F = 8.07, p < 0.01, df1 = 4, df2 = 50; Shannon: F = 45.39, p < 0.01, df1 = 4, df2 = 50). Alpha-diversity indices of samples pQ_1, pQ_R, Q_1, and Q_R is high (Fig. 2): the Simpson index approaches 1, the number of ASVs are not less than 1200. These samples are characterized by a relatively small range of indices’ values between replicates, which probably indicates general homogeneity of microbial community. Samples of group pQ_2, on the contrary, have a high range, as well as the small amount of ASVs.

Fig. 2
figure 2

Alpha-diversity indices of microbial communities

According to beta-diversity data (Fig. 3), all samples form clear clusters on the dendrogram, results of PERMANOVA shows sampling site as significant factor (bray: F = 24.7, p < 0.01, df1 = 4, df2 = 49; wunifrac: F = 23.3, p < 0.01, df1 = 4, df2 = 49). Agrochemical parameters fits well in sample distribution: according CCA analysis followed by permutational test, significant factors were pH, P and NH4+ amounts (Fig. 3).

Fig. 3
figure 3

Beta-diversity indices of communities and CCA analysis (bray - PCoA of Bray distances; wunifrac - PCoA of Weighted UniFrac distances; CCA - CCA plot)

At phyla level, all samples demonstrate similar composition of taxa. The composition of pQ_R have more Verrucomicrobia and Actinobacteria species, and less Acidobacteria and Bacteroidetes. Q_1 samples demonstrate less Planctomycetales, than reference mature soil samples Q_R. Pre-quaternary samples pQ_1 have more Bacteroidetes and less Actinobacteria, than reference samples pQ_R, whereas pQ_2 samples are highly different by i) different taxonomical composition between replicas, ii) small amount of Verrucomicrobia and Planctomycetes, presence of Firmicutes (see Fig. 4).

Fig. 4
figure 4

Relative abundance of bacterial taxa at phylum level (phyla, less abundant, than 0.01, are masked in “<0.01 abund.” group)

In comparison of unique and common ASVs in different soils the mature sandy (Q_R) and loamy (pQ_R) soils shares 43% of ASVs. 23% and 34% of ASVs are specific for both mature soils respectively. Sandy Q_1 soil have 20% ASVs as unique; pQ_1 and pQ_2 have demonstrate even less share of unique ASVs – 18% and 8% respectively (Fig. 5). More precise analyses at ASVs level reveal a range of taxa, which reflects significant differences between soil sites (Fig. 6).

Fig. 5
figure 5

Common and unique shares of ASVs in comparisons of different soils

Fig. 6
figure 6

Significant differences in comparisons of the different soils

Discussion

Our results reveal significant differences between mature and dump soils. These differences can be explained primarily by early stage of succession, both plant and microbial. Another strong factor is the nutritional properties of substrate. Despite combination of multiple factors there is possible to investigate several aspects of soil formation.

Well-developed soils are not similar in terms of microbial taxa, but functional similarity needs research. The topsoil of both pre-quaternary sod-podzolic loamy soil (pQ_R) and podzol glacial sandy soil (Q_R) are active intermediates of well-established soil processes on same region. The main nutritional factors (except P amount) do not demonstrate significant difference. In terms of microbial composition both soils have diverse community without any difference in alpha-diversity (Fig. 1). It is reasonable to suggest, that microbial communities of both soils have i) relatively big amount of unique microbial taxa due different origin of microbial community, ii) predominance of similar or even same taxa due similar nutrition and development stage.

First thesis is supported by ASVs shares (Fig. 5), where up to 23% ASVs are unique for their soils. The second thesis is more complicated: relatively high distance in beta-diversity (Fig. 3) do not allows to find similarity in microbial communities. Despite it, the similarity possibly can be revealed in analysis of metabolic pathways. Another reason could be plant-soil interaction. Different plant communities form specific rhizosphere communities [21] which leads to differences in soil microbial community. Differential taxonomic analysis in Q_R and pQ_R comparison reveals mostly common plant-associated bacterial genera, like previously described Aquispherae [22], Bradyrizobium [23] and Reyranella [24]. In this case, the difference in soil communities are connected with plants, not the soil properties themselves. This theme needs additional research.

Sand dumps are similar with mature soil, but in early stage of formation. Embryonic sandy soils (Q_1) have similar origin with reference glacial sandy soil (Q_R), and have demonstrate similar nutrition condition (Supplementary Table 1). Relatively small Bray and Unifrac distances allows to suggest similar microbial community. Despite this similarity, sand dumps are undeveloped soil. Thin AY horizon, a lot of surface litter and monogenic pine overgrown are markers of early stage of soil formation. Amount of unique ASVs for this soil is 20% (and 116 ASVs), but according small beta-diversity distance these unique ASVs are minor components of microbial community. This suggestion is supported by differential expression analysis, where abundant ASVs were found mainly in Q_R reference podzol sands. These taxa also have been previously reported as the soil taxa connected with plants. The main differences were in abundance of Aquisphaera and Roseiarcus. Aquisphaera was previously reported in water microbiomes [22, 25] and forested tundra wetlands [26], Roseiarcus was described as part of blueberry rhizosphere microbiota [27]. In addition, Edaphobacter was previously isolated from alpine and forest soils [28], and Xylophilus was described in azalea plant in Korea [29]. Acidibacter and Acidicaldus, also revealed in this comparison, are both termo- and acidophilic ferric iron-reducing bacteria [30, 31], perhaps, are result of contamination.

Dumps of refractory clays are toxic and form highly specific microbial community. Overburden loamy soil pQ_1 have been derived from regular moraine as well as reference sod-podzolic loam pQ_R. Both of these soils have been overgrown by different plants up to 20 years and have clear soil horizons. As expected, alpha-diversity of microbial communities of both soils are high, soils share about 40% (2454 ASVs) of bacterial taxa. In the same time, beta-diversity distances between samples from both soils are extremely high. This pattern can be the consequence of different evolution of soils. Being formed on same basis, both soils have formed their own microbial communities with specific abundances of similar taxa.

In contrary, soil-like mix with large unrolled rocky debris (pQ_2) do not have any signs of soil formation or plant overgrow. Large rocks, coal and oxidized pyrite particles alongside highly acidic reaction (as a result of pyrite decomposition) leads to reducing of microbial activity. As a result, alpha-diversity from pQ_2 samples are low, both alpha-metrics and relative abundance at phyla level are variable, which indicates unstable bacterial community. Due 10% share of common microbial taxa, pQ_2 samples are highly specific. Despite this, differential abundance analysis does not found any acidophilic taxa, presumably due high variance in abundances. This research should be extended in a future by specific search of acidophilic taxa.

Due differential abundance analysis limitations, mainly common soil- and plant-associated taxa were found. Plant-associated microorganisms were founded previously in rhizospheres – for example, Bradyrhyzobium [23], Nocardioides [32]. Some of the taxa previously reported as typical soil microbiota – Nocardioides [32, 33], Pseudonocardia [34, 35], Kribbella [36], Pseudolabrys [37]. Except differential analysis limitation, this result can be connected with using of topsoil. The upper soil is closely connected with plants in well-developed soils, and do not have such connection in poor soils.

Due highly specific and complicated soil-microbial-plant interactions, the first stage of any research in a new location should be brief characterization of soil and microbial changes and setting of milestones for future research.

Determined nutritional factors—pH, carbon and nitrogen amount—are previously reported as the most important factors, shaping microbial community of restored soil [38,39,40]. Moreover, in some cases changes in soil pH are more important for microbial composition, than direct addition of nutrients [41].

Dumps and mine tailing soils in most researches are describing in different reclamation aspects. Time of soil exposure also can be viewed as a part of reclamation: according reports, reclamation time was the main force driving restoration of the soil quality and bacterial community [42]. In line with our results researchers reports, that soil bacterial and fungal community structures correlated mainly with vegetation density, and plant species [43]. The exact changes in microbial community are unique for different soils and areas. For example, in coal mining dumps relative abundance of Proteobacteria, Actinobacteria and Bacteroidetes was increased, while the one of Acidobacteria, Chloroflexi and Nitrospirae – decreased [42], while in our research the relative abundance of Proteobacteria were same, Acidobacteria and Bacteroidetes were ambivalent. The particular taxa included in restoration processes presumably also are unique for different soils: for example, in research of acidogenic mine tailings Acidiferrobacter, Leptospirillum (in location without plant overgrown) and Bradyrhizobium (in overgrown tailings) were reported as significant taxa. In our research Bradyrhizobium was found in mature soil. In acid fresh mine soils, the iron/sulfur-oxidizers such as Acidiferrobacter and Sulfobacillus were reported [44].

Conclusions

Microbial communities of soils and dumps are variable and different in terms both nutritional and microbial components. PH, N and TOC are strong predictors for microbial composition.

Microbial communities of well-developed pre-quaternary and quaternary soils are different, possible functional similarity needs research. Dumps of refractory clays pQ_2 are non-developed, highly acidic and form specific microbial community. Differential abundance analysis does not found any acidophilic taxa, presumably due high variance in abundances. This research should be extended in a future by specific search of acidophilic taxa.

In comparison of dumps and mature soils in both pre-quaternary and quaternary soils we estimate specific bacterial taxa. They are connected more with plant composition, not the soil properties themselves. Except differential analysis limitation, this result can be connected with using of topsoil layer.

The exact changes in microbial community are unique for different soils and areas. Analysis of main nutrition components and 16S amplicon sequencing allow to find ways for more targeted research of different aspects and form specific hypothesis.

Availability of data and materials

The datasets generated and analyzed during the current study are available in the SRA repository, https://www.ncbi.nlm.nih.gov/sra/PRJNA705583.

Abbreviations

ASV:

Amplicon Sequence Variant

WRB:

World Reference Base (for Soil Resources)

References

  1. Bardina T, Chugunova M, Kulibaba V, Polyak Y, Bardina V, Kapelkina L. Applying Bioassay Methods for Ecological Assessment of the Soils from the Brownfield Sites. Water Air Soil Pollut. 2017;228:351.

    Article  Google Scholar 

  2. Vicentini F, Hendrychová M, Tajovský K, Pižl V, Frouz J. The Effect of Topography on Long-Term Spontaneous Development of Soil and Woody Cover on Graded and Untreated Overburden. Forests. 2020;11:602.

    Article  Google Scholar 

  3. Hüblová L, Frouz J. Contrasting effect of coniferous and broadleaf trees on soil carbon storage during reforestation of forest soils and afforestation of agricultural and post-mining soils. J Environ Manage. 2021;290:112567.

    Article  Google Scholar 

  4. Veselá H, Lhotakova Z, Albrechtová J, Frouz J. Seasonal changes in tree foliage and litterfall composition at reclaimed and unreclaimed post-mining sites. Ecol Eng. 2021;173(4).

  5. Kimeklis AK, Gladkov GV, Zverev AO, Kichko AA, Andronov EE, Ergina EI, Kostenko IV, Abakumov EV. Microbiomes of different ages in Rendzic Leptosols in the Crimean Peninsula. PeerJ. 2021;9:e10871.

  6. Lin Q, Dini-Andreote F, Li L, Umari R, Novotny V, Kukla J, et al. Soil microbial interconnections along ecological restoration gradients of lowland forests after slash-and-burn agriculture. FEMS Microbiol Ecol. 2021;97(5).

  7. Pershina E, Ivanova E, Kineklis A, Zverev A, Kichko A, Aksenova T, et al. Soil microbiomes of reclaimed and abandoned mines of the Yamal region. Polish Polar Res. 2020;41:95–114.

    Google Scholar 

  8. Woś B, Józefowska A, Paj\k ak M, Chodak M, Frouz J, Pietrzykowski M. Carbon and Macronutrient Budgets in an Alder Plantation Grown on a Reclaimed Combustion Waste Landfill. Forests. 2020;11:430.

    Article  Google Scholar 

  9. Cejpek J, Kuráž V, Vindušková O, Frouz J. Water regime of reclaimed and unreclaimed post‐mining sites. Ecohydrology. 2017;11(6).

  10. Gladkov G, Chebykina E, Evdokimova E, Ivanova E, Kimeklis A, Zverev A, et al. Restoration of soil microbiome in various soil horizons after crown and surface wildfires. Ecol Genet. 2020;18(3).

  11. Ivanova E, Pershina E, Karpova D, Rogova O, Abakumov E, Andronov E. Soil microbiome in chronosequence of spoil heaps of Kursk Magnetic Anomaly. Biol Commun. 2019;64(3).

  12. FAQ. Standard operating procedure for soil pH determination [Internet]. Rome. Italy: FAQ; 2021. Available from: https://www.fao.org/publications/card/en/c/CB3637EN

  13. FAQ. Standard operating procedure for soil available phosphorus - Olsen method [Internet]. Rome. Italy: FAQ; 2021. Available from: https://www.fao.org/publications/card/en/c/CB3644EN

  14. Munson R, Lean E, Watson ME. Soil Measurements of Plant-Available Potassium. In 1985.

  15. Caporaso J, Lauber C, Walters W, Berg-Lyons D, Lozupone C, Turnbaugh P, et al. Global patterns of 16S rRNA diversity at a depth of millions of sequences per sample. Proc Natl Acad Sci U S A. 2011;108(Suppl):4516–22.

    Article  CAS  Google Scholar 

  16. Callahan B, Mcmurdie P, Rosen M, Han A, Johnson AJ, Holmes S. DADA2: High-resolution sample inference from Illumina amplicon data. Nat Methods. 2016;13(7).

  17. Quast C, Pruesse E, Yilmaz P, Gerken J, Schweer T, Yarza P, et al. The SILVA ribosomal RNA gene database project: improved data processing and web-based tools. Nucleic Acids Res. 2013;41:D590–6.

    Article  CAS  Google Scholar 

  18. Mcmurdie P, Holmes S. Phyloseq: An R Package for Reproducible Interactive Analysis and Graphics of Microbiome Census Data. PLoS ONE. 2013;8:e61217.

    Article  CAS  Google Scholar 

  19. Love M, Huber W, Anders S. Moderated estimation of fold change and dispersion for RNA-Seq data with DESeq2. Genome Biol. 2014;15:550.

    Article  Google Scholar 

  20. Oksanen J, Blanchet FG, Kindt R, Legendre P, Minchin P, O’Hara B, et al. Vegan: Community Ecology Package. R Packag Version. 2015;22–1(2):1–2.

    Google Scholar 

  21. Zverev AO, Kichko AA, Pinaev AG, Provorov NA, Andronov EE. Diversity Indices of Plant Communities and Their Rhizosphere Microbiomes: An Attempt to Find the Connection. Microorganisms. 2021;9(11):2339.

  22. Gaurav K, Lhingjakim K, Uppada J, Ahmad S, Kumar D, Gulam Mohd K, et al. Aquisphaera insulae sp. nov., a new member in the family Isosphaeraceae, isolated from the floating island of Loktak lake and emended description of the genus Aquisphaera. Antonie Van Leeuwenhoek. 2021;114(W1).

  23. Shah V, Subramaniam S. Bradyrhizobium japonicum USDA110: A representative model organism for studying the impact of pollutants on soil microbiota. Sci Total Environ. 2017;624:963–7.

    Article  Google Scholar 

  24. Kim S-J, Ahn J-H, Lee T-H, Weon H-Y, Hong S-B, Seok S-J, et al. Reyranella soli sp nov., isolated from forest soil, and emended description of the genus Reyranella Pagnier et al. 2011. Int J Syst Evol Microbiol. 2013;63(Pt 9).

  25. Bondoso J, Albuquerque L, Nobre M, Lobo-da-Cunha A, da Costa M, Lage O. Aquisphaera giovannonii gen nov., sp nov., a planctomycete isolated from a freshwater aquarium. Int J Syst Evol Microbiol. 2011;61:2844–50.

    Article  CAS  Google Scholar 

  26. Kulichevskaya I, Ivanova A, Suzina N, Rijpstra I, Sinninghe-Damste J, Dedysh S. Paludisphaera borealis gen. nov., sp. nov., a hydrolytic planctomycete from northern wetlands, and the proposal of Isosphaeraceae fam. nov. Int J Syst Evol Microbiol. 2016;66:837–44.

    Article  CAS  Google Scholar 

  27. Morvan S, Meglouli H, Lounès-Hadj Sahraoui A, Hijri M. Into the wild blueberry (Vaccinium angustifolium) rhizosphere microbiota. Environ Microbiol. 2020;22.9:803-3822.

  28. Koch I, Gich F, Dunfield P, Overmann J. Edaphobacter modestus gen. nov., sp. nov., and Edaphobacter aggregans sp. nov., Acidobacteria isolated from alpine and forest soils. Int J Syst Evol Microbiol. 2008;58:1114–22.

    Article  CAS  Google Scholar 

  29. Lee S, Heo J, Kim T-W, Sang MK, Song J, Kwon S-W, et al. Xylophilus rhododendri sp. nov., Isolated from Flower of Royal Azalea, Rhododendron schlippenbachii. Curr Microbiol. 2020;77(12).

  30. Falagan C, Johnson D. Acidibacter ferrireducens gen. nov., sp. nov.: an acidophilic ferric iron-reducing gammaproteobacterium. Extremophiles. 2014;18(6).

  31. Johnson D, Stallwood B, Kimura S. Isolation and characterization of Acidicaldus organivorus, gen. nov., sp. nov.: A novel sulfur-oxidizing, ferric iron-reducing thermo-acidophilic heterotrophic Proteobacterium. Arch Microbiol. 2006;185:212–21.

    Article  CAS  Google Scholar 

  32. Suh M, Lee K, Kim J, Han K-I, Kim H, Eom M, et al. Nocardioides cynanchi sp. nov., isolated from soil of rhizosphere of Cynanchum wilfordii. Int J Syst Evol Microbiol. 2021;71(2).

  33. Park Y, Liu Q, Maeng S, Choi W, Chang Y, Im WT. Nocardioides convexus sp. nov. and Nocardioides anomalus sp. nov., isolated from soil and mineral water. Int J Syst Evol Microbiol. 2020;70(12).

  34. Chanama S, Janphen S, Suriyachadkun C, Chanama M. Pseudonocardia mangrovi sp. Nov., isolated from soil. Int J Syst Evol Microbiol. 2018;68(9).

  35. Thawai C. Pseudonocardia soli sp. nov., isolated from mountain soil. Int J Syst Evol Microbiol. 2018;68(4).

  36. Song W, Duan L, Zhao J, Jiang S, Guo X, Xiang W, et al. Kribbella monticola sp. nov., a novel actinomycete isolated from soil. Int J Syst Evol Microbiol. 2018;68:3441–6.

    Article  CAS  Google Scholar 

  37. Kämpfer P, Chiu-Chung Y, AB A, Shen F-T, Jäckel U, Rossello-Mora R, et al. Pseudolabrys taiwanensis gen. nov., sp. nov., an alphaproteobacterium isolated from soil. Int J Syst Evol Microbiol. 2006;56(Pt 10):2469-72.

  38. Sun R, Zhang X-X, Guo X, Wang D, Chu H. Bacterial diversity in soils subjected to long-term chemical fertilization can be more stably maintained with the addition of livestock manure than wheat straw. Soil Biol Biochem. 2015;88:9-18.

  39. Hartmann M, Frey B, Mayer J, Mäder P, Widmer F. Distinct soil microbial diversity under long-term organic and conventional farming. ISME J. 2014;9(5).

  40. Kane J, Morrissey E, Skousen J, Freedman Z. Soil microbial succession following surface mining is governed primarily by deterministic factors. FEMS Microbiol Ecol. 2020;96(11).

  41. Kavamura V, Hayat R, Clark I, Rossmann M, Mendes R, Hirsch P, et al. Inorganic Nitrogen Application Affects Both Taxonomical and Predicted Functional Structure of Wheat Rhizosphere Bacterial Communities. Front Microbiol. 2018;9:1074.

    Article  Google Scholar 

  42. Wang X, Li Y, Wei Y, Meng H, Cao Y, Lead JR, et al. Effects of fertilization and reclamation time on soil bacterial communities in coal mining subsidence areas. Sci Total Environ. 2020;739:139882.

    Article  CAS  Google Scholar 

  43. Gagnon V, Rodrigue-Morin M, Tremblay J, Wasserscheid J, Champagne J, Bellenger J-P, et al. Vegetation drives the structure of active microbial communities on an acidogenic mine tailings deposit. PeerJ. 2020;8:e10109.

    Article  Google Scholar 

  44. Zhang Q, Wei P, Banda J, Ma L, Mao W, Li H, et al. Succession of Microbial Communities in Waste Soils of an Iron Mine in Eastern China. Microorganisms. 2021;9:2463.

    Article  CAS  Google Scholar 

Download references

Acknowledgements

Not applicable.

Funding

This work was supported by the Ministry of Science and Higher Education of the Russian Federation in accordance with agreement № 075-15-2022-322 date 22 April 2022 on providing a grant in the form of subsidies from the Federal budget of Russian Federation. The grant was provided for state support for the creation and development of a World-class Scientific Center “Agrotechnologies for the Future”.

Author information

Authors and Affiliations

Authors

Contributions

AZ interpreted and analyzed data, wrote the manuscript, AKm and GG collected samples, AKch sequenced samples, EAn, EAb acquired funding and provided equipment and supervising. The author(s) read and approved the final manuscript.

Corresponding author

Correspondence to Aleksei Zverev.

Ethics declarations

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Additional file 1: Supplementary Table 1.

Agrochemical analysis of soils.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Zverev, A., Kimeklis, A., Kichko, A. et al. Microbial features of mature and abandoned soils in refractory clay deposits. BMC Microbiol 22, 237 (2022). https://doi.org/10.1186/s12866-022-02634-7

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12866-022-02634-7

Keywords

  • 16S amplicons
  • Abandoned soils
  • Anthropogenically disturbed soils
  • Microbiome analysis
  • Soil biodiversity
  • Soil microbiome