Abstract
Changes in the nitrogen (N) and phosphorus (P) content in the ash substrate and plant leaves during the primary succession of overgrowing ash dumps of different ages were studied. The work was carried out on the young (overgrowth duration 5–8 years) and old (overgrowth duration 53–56 years; two sites – with meadow and forest vegetation) ash dumps of a thermal power plant in the Middle Urals. In the emerging soil and leaves of model plants, the content of N and P was determined on each dump. In young soils, a predictable and explainable successional dynamics of N and P was established: over 53–56 years, the N content increased 2.4–7.1 times, while the P content decreased 1.1–2.1 times. In plant leaves, the content of N and P at different stages of overgrowth was actually constant: 1.6–2.1% of N and 2.2–2.9 mg/g of P. In general, it has been found that in successionally young habitats, and in more advanced ones with develo** forest vegetation, against the background of a multiple increase in the N content in the soil, the N content in plants remains low. With a high probability, on both dumps, the availability of nitrogen is a factor limiting the development of plants. This is evidenced by the results of the analysis of N/P ratio values in leaves and comparison of our array of N values in leaves with global averages of N content in the same species. Thus, the results with respect to the successional dynamics of the content of nitrogen and phosphorus in soils and plants of dumps of different ages turned out to be surprisingly little consistent with each other.
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REFERENCES
Elser, J.J., Bracken, M.E.S., Cleland, E.E., et al., Global analysis of nitrogen and phosphorus limitation of primary producers in freshwater, marine and terrestrial ecosystems, Ecol. Lett., 2007, vol. 10, no. 12, pp. 1135–1142. https://doi.org/10.1111/j.1461-0248.2007.01113.x
Bui, E.N. and Henderson, B.L., C : N : P stoichiometry in Australian soils with respect to vegetation and environmental factors, Plant Soil, 2013, vol. 373, pp. 553–568. https://doi.org/10.1007/s11104-013-1823-9
Chapin, F.S., Vitousek, P.M., and Cleve, K., The nature of nutrient limitation in plant communities, Am. Nat., 1986, vol. 127, pp. 48–58.
Aerts, R. and Chapin, F.S., The mineral nutrition of wild plants revisited: A re-evaluation of processes and patterns, Adv. Ecol. Res., 2000, vol. 30, pp. 1–67. https://doi.org/10.1016/S0065-2504(08)60016-1
Wang, G., Leaf trait co-variation, response and effect in a chronosequence, J. Veg. Sci., 2007, vol. 18, no. 4, pp. 563–570. https://doi.org/10.1111/j.1654-1103.2007.tb02570.x
He, M., Dijkstra, F.A., and Zhang, K., Leaf nitrogen and phosphorus of temperate desert plants in response to climate and soil nutrient availability, Sci. Rep., 2014, vol. 4, p. 6932.
Soudzilovskaia, N.A., Onipchenko, V.G., Cornelissen, J.H.C., et al., Biomass production, N : P ratio and nutrient limitation in a Caucasian alpine tundra plant community, J. Veg. Sci., 2005, vol. 16, pp. 399–406. https://doi.org/10.1111/j.1654-1103.2005.tb02379.x
von Oheimb, G., Power, S.A., Falk, K., et al., N : P Ratio and the nature of nutrient limitation in Calluna-dominated heathlands, Ecosystems, 2010, vol. 13, pp. 317–327. https://doi.org/10.1007/s10021-010-9320-y
Liu, B., Han, F., Ning, P., et al., Root traits and soil nutrient and carbon availability drive soil microbial diversity and composition in a northern temperate forest, Plant Soil, 2022, vol. 479, pp. 281–299. https://doi.org/10.1007/s11104-022-05516-z
Ning, Z., Zhao, X., Yulin, L., et al., Plant community C : N : P stoichiometry is mediated by soil nutrients and plant functional groups during grassland desertification, Ecol. Eng., 2021, vol. 162, no. 1, pp. 106–179. https://doi.org/10.1016/j.ecoleng.2021.106179
Yan, T., Lu, X.-T., Zhu, J.-J., et al., Changes in nitrogen and phosphorus cycling suggest a transition to phosphorus limitation with the stand development of larch plantations, Plant Soil, 2018, vol. 422, pp. 385–396. https://doi.org/10.1007/s11104-017-3473-9
Peltzer, D.A., Wardle, D.A., Allison, V.J., et al., Understanding ecosystem retrogression, Ecol. Monogr., 2010, vol. 80, no. 4, pp. 509–529. https://doi.org/10.1890/09-1552.1
Makhonina, G.I., Ekologicheskie aspekty pochvoobrazovaniya v tekhnogennykh ekosistemakh Urala (Ecological aspects of soil formation in technogenic ecosystems of the Urals), Yekaterinburg: Ural. Univ., 2003.
Vitousek, P.M., Nutrient Cycling and Limitation: Hawaii as a Model System, Princeton: Princeton Univ. Press, 2004.
Laliberte, E., Turner, B.L., Costes, T., et al., Experimental assessment of nutrient limitation along a 2-million year dune chronosequence in the south-western Australia biodiversity hotspot, J. Ecol., 2012, vol. 100, pp. 631–642. https://doi.org/10.1111/j.1365-2745.2012.01962.x
Coomes, D.A., Bentley, W.A., Tanentzap, A.J., et al., Soil drainage and phosphorus depletion contribute to retrogressive succession along a New Zealand chronosequence, Plant Soil, 2013, vol. 367, pp. 77–91.https://doi.org/10.1007/s11104-013-1649-5
Olde Venterink, H. and Gusewell, S., Competitive interactions between two meadow grasses under nitrogen and phosphorus limitation, Funct. Ecol., 2010, vol. 24, pp. 877–886. https://doi.org/10.1111/j.1365-2435.2010.01692.x
Darcy, J.L., Schmidt, S.K., and Knelman, J.E., Phosphorus, not nitrogen, limits plants and microbial primary producers following glacial retreat, Sci. Adv., 2018, vol. 4, no. 5, p. eaaq0942. https://doi.org/10.1126/sciadv.aaq0942
Satti, P.P., Mazzarino, M.J., and Roselli, L., Factors affecting soil P dynamics in temperate volcanic soils of southern Argentina, Geoderma, 2007, vol. 139, pp. 229–240.
Hayes, P.E., Turner, B.L., Lambers, H., et al., Foliar nutrient concentrations and resorption efficiency in plants of contrasting nutrient-acquisition strategies along a 2-million-year dune chronosequence, J. Ecol., 2014, vol. 102, pp. 396–410. https://doi.org/10.13140/2.1.5050.4968
Zhong, H., Zhou, J., Wong, W.-S., et al., Exceptional nitrogen-resorption efficiency enables Maireana species (Chenopodiaceae) to function as pioneers at a mine-restoration site, Sci. Total Environ., 2021, vol. 779, p. 146420. https://doi.org/10.1016/j.scitotenv.2021.146420
Read, D.J. and Perez-Moreno, J., Mycorrhizas and nutrient cycling in ecosystems—A journey towards relevance?, New Phytol., 2003, vol. 157, pp. 475–492. https://doi.org/10.1046/j.1469-8137.2003.00704.x
Dickie, I.A., Martinez-Garcia Laura, B., Koele, N., et al., Mycorrhizal and mycorrhizal fungal communities throughout ecosystem development, Plant Soil, 2013, vol. 367, pp. 11–39.https://doi.org/10.1007/s11104-013-1609-0
Koerselman, W. and Meuleman, A.F.M., The vegetation N : P ratio: A new tool to detect the nature of nutrient limitation, J. Appl. Ecol., 1996, vol. 33, no. 6, pp. 1441–1450. http://www.jstor.org/stable/2404783
Güsewell, S., N : P ratios in terrestrial plants: Variation and functional significance, New Phytol., 2004, vol. 164, pp. 243–266. https://doi.org/10.1111/j.1469-8137.2004.01192.x
Pasynkova, M.V., Ash as a substrate for growing plants, in Rasteniya i promyshlennaya sreda (Plants and Industrial Environment), Sverdlovsk: Ural. Gos. Univ., 1974, pp. 29–44.
Gajić, G., Djurdjević, L., Kostić, O., et al., Ecological potential of plants for phytoremediation and ecorestoration of fly ash deposits and mine wastes, Front. Environ., 2018, vol. 6, p. 124. https://doi.org/10.3389/fenvs.2018.00124
The Plant List. http://www.theplantlist.org/. Cited November 21, 2022.
Arinushkina, E.V., Rukovodstvo po khimicheskomu analizu pochv (Guide to the Chemical Analysis of Soils), Moscow: Mosk. Gos. Univ., 1970.
Teoriya i praktika khimicheskogo analiza pochv (Theory and Practice of Chemical Analysis of Soils), Vorob’ev, L.A., Ed., Novosibirsk: GEOS, 2006.
Kattge, J., Boenisch, G., Diaz, S., et al., TRY plant trait database – enhanced coverage and open access, Global Change Biol., 2020, no. 26, pp. 119–188. https://doi.org/10.1111/gcb.14904
Wang, B. and Qiu, Y.L., Phylogenetic distribution and evolution of mycorrhizas in land plants, Mycorrhiza, 2006, vol. 16, no. 5, pp. 299–363.
Akhmetzhanova, A.A., Soudzilovskaia, N.A., Onipchenko, V.G., et al., A rediscovered treasure: Mycorrhizal intensity database for 3000 vascular plant species across the former Soviet Union, Ecology, 2012, vol. 93, no. 3, pp. 689–690. https://doi.org/10.1890/11-1749.1
Betekhtina, A.A. and Veselkin, D.V., Prevalence and intensity of mycorrhiza formation in herbaceous plants with different types of ecological strategies in the Middle Urals, Russ. J. Ecol., 2011, vol. 42, no. 3, pp. 192–198.https://doi.org/10.1134/S1067413611030040
Betekhtina, A.A. and Veselkin, D.V., Mycorrhizal and non-mycorrhizal dicotyledonous herba-ceous plants differ in root anatomy: Evidence from the Middle Urals, Russia, Symbiosis, 2019, vol. 77, no. 2, pp. 133–140. https://doi.org/10.1007/s13199-018-0571-2
Gadzhiev, I.M. and Kurachev, V.M., Genetic and ecological aspects of the study and classification of soils in technogenic landscapes, in Ekologiya i rekul’tivatsiya tekhnogennykh landshaftov (Ecology and Reclamation of Technogenic Landscapes), Novosibirsk: Nauka, 1992, pp. 6–15.
IUSS Working Group WRB. World Reference Base for Soil Resources. International soil classification system for naming soils and creating legends for soil maps, Vienna: International Union of Soil Sciences (IUSS), 2022.
Cornelissen, J.H.C., Aerts, R., Cerabolini, B., et al., Carbon cycling traits of plant species are linked with mycorrhizal strategy, Oecologia, 2001, vol. 129, no. 4, pp. 611–619.
Walker, T.W. and Syers, J.K., The fate of phosphorus during pedogenesis, Geoderma, 1976, vol. 15, pp. 1–19.
Nazaryuk, V.M. and Kalimullina, F.R., The role of natural ecosystems in restoring the fertility of plowed soils in Western Siberia, Probl. Agrokhim. Ekol., 2017, no. 1, pp. 43–50.
Komarov, A., Chertov, O., Bykhovets, S.S., et al., Effects of the aspen short-rotation plantation on the C and N biological cycles in boreal forests: The model experiment, Math. Biol. Bioinf., 2015, vol. 10, no. 2, pp. 398–415. https://doi.org/10.17537/2015.10.398
Betekhtina, A.A., Nekrasova, O.A., Radchenko, T.A., et al., Decomposition of meadow and forest plant roots in the Ash substrate of power plant dumps: A laboratory experiment, Biol. Bull., 2020, vol. 47, no. 3, pp. 299–305.https://doi.org/10.1134/S1062359020010033
Betekhtina, A.A., Ganem, A., Nekrasova, O.A., et al., Factors of carbon and nitrogen contents in the fine roots of plants in the Middle Urals, Russ. J. Ecol., 2021, vol. 52, no. 2, pp. 99–108.https://doi.org/10.1134/S106741362102003X
Ghafoor, A., Poeplau, C., and Kätterer, T., Fate of straw- and root-derived carbon in a Swedish agricultural soil, Biol. Fertil. Soils, 2017, vol. 53, no. 2, pp. 257–267. https://doi.org/10.1007/s00374-016-1168-7
Poirier, V., Roumet, C., and Munson, A.D., The root of the matter: Linking root traits and soil organic matter stabilization processes, Soil Biol. Biochem., 2018, vol. 120, pp. 246–259. https://doi.org/10.1016/j.soilbio.2018.02.016
Makarov, M.I., The role of mycorrhiza in transformation of nitrogen compounds in soil and nitrogen nutrition of plants: A review, Eurasian Soil Sci., 2019, vol. 52, no. 2, pp. 193–205.https://doi.org/10.1134/S1064229319100077
Makarov, M.I., Lavrenov, N.G., and Onipchenko, V.G., Nitrogen nutrition of plants in an Alpine lichen heath under the conditions of soil enrichment with biogenic elements, Russ. J. Ecol., 2020, vol. 51, no. 2, pp. 99–106.https://doi.org/10.1134/S1067413620020083
Cross, A.T. and Lambers, H., Young calcareous soil chronosequences as a model for ecological restoration on alkaline mine tailings, Sci. Total Environ., 2017, vols. 607–608, pp. 168–175. https://doi.org/10.1016/j.scitotenv.2017.07.005
Crews, T.E., Kitayama, K., Fownes, J.H., et al., Changes in soil phosphorus fractions and ecosystem dynamics across a long chronosequence in Hawaii, Ecology, 1995, vol. 76, pp. 1407–1424. https://doi.org/10.2307/1938144
Satti, P.P., Mazzarino, M.J., Roselli, L., et al., Factors affecting soil P dynamics in temperate volcanic soils of southern Argentina, Geoderma, 2007, vol. 139, nos. 1 2, pp. 229–240. https://doi.org/10.1016/j.geoderma.2007.02.005
Makarov, M.I., Phosphorus in soil organic matter, Extended Abstract of Doctoral (Biol.) Dissertation, Moscow, 2004.
Kraus, T.E., Dahlgren, R.A., and Zasoski, R.J., Tannins in nutrient dynamics of forest ecosystems—A review, Plant Soil, 2003, vol. 256, no. 1, pp. 41–66. https://doi.org/10.1023/A:1026206511084
Mallik, A.U., Conifer regeneration problems in boreal and temperate forest with ericaceous understory: Role of disturbance, seedbed limitation, and keystone change, Crit. Rev. Plant Sci., 2003, vol. 22, pp. 341–366.
Dergacheva, M.I., Sistema gumusovykh veshchestv pochv (The System of Humic Substances in Soils), Novosibirsk: Nauka, 1989.
Brady, N.C. and Well, R.R., Elementos da Natureza e Propriedades dos Solos, Porto Alegre: Bookman, 2013.
Vergutz, L., Manzoni, S., Porporato, A., et al., Global resorption efficiencies and concentrations of carbon and nutrients in leaves of terrestrial plants, Ecol. Monogr., 2012, vol. 82, pp. 205–220.
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The study was carried out with the financial support of the Ministry of Science and Higher Education of the Russian Federation within the Development Program of the Ural Federal University in accordance with the program of strategic academic leadership Priority-2030; geobotanical research and plant analysis were carried out within the state task (subject No. FEUZ-2023-0023).
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Betekhtina, A., Nekrasova, O., Uchaev, A. et al. Over 50 Years of Overgrowth of the Ash Dump, The Content of Nitrogen and Phosphorus Changed in Young Soils but it Did Not Change in Plants. Russ J Ecol 54, 287–296 (2023). https://doi.org/10.1134/S1067413623040045
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DOI: https://doi.org/10.1134/S1067413623040045