Воронеж, Воронежская область, Россия
УДК 631.46 Бактериология и биология почв
Проведен обзор исследований, который показал, что микоризный симбиоз играет ключевую роль в устойчивости экосистем, влияя на круговорот веществ и секвестрацию углерода. Разные типы микоризы по-разному воздействуют на биогеохимические циклы и продуктивность растений. Искусственная микоризация эффективна на бедных почвах, повышая выживаемость древесных пород, что делает её перспективной в лесовосстановлении и адаптации к изменению климата.
микориза; микоризный симбиоз; эктомикориза; арбускулярная микориза; биогеохимические циклы; секвестрация углерода; лесовосстановление; рекультивация; устойчивость растений
1. Бурцев Д. С. Зарубежный опыт искусственной микоризации сеянцев лесных древесных пород с закрытой корневой системой // Труды Санкт-Петербургского научно-исследовательского института лесного хозяйства. – 2014. – № 1.
2. Елеусенова Н. Г., Селиванов И. А. Микотрофность растений во флоре северных пустынь Казахстана // Учен. зап. Пермск. пед. ин-та. – 1973. – Т. 112.
3. Иозус А. П., Завьялов А. А., Бойко С. Ю. Особенности влияния микоризы на приживаемость и биохимический состав сеянцев сосны обыкновенной в сухой степи Нижнего Поволжья // Успехи современного естествознания. – 2019. – № 6. – С. 23–27.
4. Костычев П. А. Состав органических веществ почвы в связи с вопросом о полезности микориз // Труды Санкт-Петербургского общества естествоиспытателей. – 1891. – Т. 21.
5. Саляев Р. К. Корни в коре // Природа : ежемесячный популярный естественно-научный журнал АН СССР. – 1961. – № 2. – С. 38.
6. Averill C. Divergence in plant and microbial allocation strategies explains continental patterns in microbial allocation and biogeochemical fluxes // Ecology Letters. – 2014. – Vol. 17. – P. 1202–1210.
7. Averill C., Anthony M. A., Baldrian P., Finkbeiner F., van den Hoogen J., Kiers T., Kohout P., Hirt E., Smith G. R., Crowther T. W. Defending Earth’s terrestrial microbiome // Nature Microbiology. – 2022. – Vol. 7. – P. 1717–1725.
8. Asmelash F., Bekele T., Birhane E. The potential role of arbuscular mycorrhizal fungi in the restoration of degraded lands // Frontiers in Microbiology. – 2016. – Vol. 7. – Article 1095.
9. Bhardwaj A. K., Chandra K. K., Kumar R. Mycorrhizal inoculation under water stress conditions and its influence on the benefit of host–microbe symbiosis of Terminalia arjuna species // Bulletin of the National Research Centre. – 2023. – Vol. 47. – P. 1–13.
10. Booth M. G. Mycorrhizal networks mediate overstorey–understorey competition in a temperate forest // Ecology Letters. – 2004. – Vol. 7. – P. 538–546.
11. Bonfante P., Genre A. Mechanisms underlying beneficial plant–fungus interactions in mycorrhizal symbiosis // Nature Communications. – 2010. – Vol. 1. – Article 48.
12. Brundrett M. C. Mycorrhizal associations and other means of nutrition of vascular plants: understanding the global diversity of host plants by resolving conflicting information and developing reliable means of diagnosis // Plant and Soil. – 2009. – Vol. 320. – P. 37–77.
13. Bödeker I. T. M. Functional Ecology of Ectomycorrhizal Fungi : Doctoral Thesis. – Uppsala : Swedish University of Agricultural Sciences, 2012. – 36 p.
14. Cairney J. W. G., Meharg A. A. Interactions between ectomycorrhizal fungi and soil saprotrophs: implications for decomposition of organic matter in soils and degradation of organic pollutants in the rhizosphere // Canadian Journal of Botany – Revue Canadienne de Botanique. – 2002. – Vol. 80. – P. 803–809.
15. Carteron A., Vellend M., Laliberté E. Mycorrhizal dominance reduces local tree species diversity across US forests // Nature Ecology & Evolution. – 2022. – Vol. 6. – P. 370–374.
16. Chen J., Wang L., Liang X., Li B., He Y., Zhan F. An arbuscular mycorrhizal fungus differentially regulates root traits and cadmium uptake in two maize varieties // Ecotoxicology and Environmental Safety. – 2023. – Vol. 264. – Article 115458.
17. Chandra K. K., Kumar R. Forestry Practicals. – Jodhpur : Scientific Publisher, 2023.
18. Dickie I. A., Montgomery R. A., Reich P. B., Schnitzer S. A. Physiological and phenological responses of oak seedlings to oak forest soil in the absence of trees // Tree Physiology. – 2007. – Vol. 27. – P. 133–140.
19. Ding Q., Liang Y., Legendre P., He X., Pei K., Du X., Ma K. Diversity and composition of ectomycorrhizal community on seedling roots: the role of host preference and soil origin // Mycorrhiza. – 2011. – Vol. 21. – P. 669–680.
20. Deng C., Zou Y. N., Hashem A., Kuca K., Abd-Allah E. F., Wu Q. S. The visualized knowledge map and hot topic analysis of glomalin-related soil proteins in the carbon field based on Citespace // Chemical and Biological Technologies in Agriculture. – 2023. – Vol. 10. – Article 48.
21. Faghihinia M., Jansa J., Halverson L. J., Staddon P. L. Hyphosphere microbiome of arbuscular mycorrhizal fungi: a realm of unknowns // Biology and Fertility of Soils. – 2023. – Vol. 59. – P. 17–34.
22. Fini A., Frangi P., Amoroso G., Piatti R., Faoro M., Bellasio C., Ferrini F. Effect of controlled inoculation with specific mycorrhizal fungi from the urban environment on growth and physiology of containerized shade tree species growing under different water regimes // Mycorrhiza. – 2011. – Vol. 21. – P. 703–719.
23. Francis M. Martin, Stéphane Uroz, David G. Barker. Ancestral alliances: Plant mutualistic symbioses with fungi and bacteria // Science. – 2017. – Vol. 356. – P. 819.
24. Gardner T. G., Frene J. P., Lawson S. S., Lue Sue N. D., Handy J., Crawford R. H. The impact of tree species on microbial community structure and soil function on forest plantations in the Central Hardwoods Region (CHR) // Forests. – 2023. – Vol. 14. – Article 859.
25. Gao Q., Yang Z. L. Ectomycorrhizal fungi associated with two species of Kobresia in an alpine meadow in the eastern Himalaya // Mycorrhiza. – 2010. – Vol. 20, № 4. – P. 281–287.
26. Giovannetti M., Tolosano M., Volpe V., Kopriva S., Bonfante P. Identification and functional characterization of a sulfate transporter induced by both sulfur starvation and mycorrhiza formation in Lotus japonicus // New Phytologist. – 2014. – Vol. 204. – P. 609–619.
27. Goebel M., Hobbie S. E., Bulaj B., Zadworny M., Archibald D. D., Oleksyn J., Reich P. B., Eissenstat D. M. Decomposition of the finest root branching orders: linking belowground dynamics to fine-root function and structure // Ecological Monographs. – 2011. – Vol. 81, № 1. – P. 89–102.
28. Grover M., Ali S. Z., Sandhya V., Rasul A., Venkateswarlu B. Role of microorganisms in adaptation of agriculture crops to abiotic stresses // World Journal of Microbiology and Biotechnology. – 2011. – Vol. 27. – P. 1231–1240.
29. Guy P., Richard S., Simon M. S., Tibbett M., Pickles B. J. Mycorrhizal type of woody plants influences understory species richness in British broadleaved woodlands // New Phytologist. – 2022.
30. Hart M. M., Antunes P. M., Chaudhary V. B., Abbott L. K. Fungal inoculants in the field: is the reward greater than the risk? // Functional Ecology. – 2018. – Vol. 32. – P. 126–135.
31. Haskins K. E., Gehring C. A. Evidence for mutualist limitation: the impacts of conspecific density on the mycorrhizal inoculum potential of woodland soils // Oecologia. – 2005. – Vol. 145. – P. 123–131.
32. Hawkins H. J., Cargill R. I., Van Nuland M. E., Hagen S. C., Field K. J., Sheldrake M., Soudzilovskaia N. A., Kiers E. T. Mycorrhizal mycelium as a global carbon pool // Current Biology. – 2023. – Vol. 33. – P. R560–R573.
33. Hobbie S. E., Reich P. B., Oleksyn J., Ogdahl M., Zytkowiak R., et al. Tree species effects on decomposition and forest floor dynamics in a common garden // Ecology. – 2006. – Vol. 87. – P. 2288–2297.
34. Högberg H. T., Sobanski T., Novellino A., Whelan M., Weiss D. G., Bal-Price A. K. Application of microelectrode arrays (MEAs) as an emerging technology for developmental neurotoxicity: evaluation of domoic acid-induced effects in primary cultures of rat cortical neurons // Neurotoxicology. – 2010.
35. Hoeksema J. D., Bever J. D., Chakraborty S., Chaudhary V. B., Gardes M., Gehring C. A., Hart M. M., Housworth E. A., Kaonongbua W., Klironomos J. N. Evolutionary history of plant hosts and fungal symbionts predicts the strength of mycorrhizal mutualism // Communications Biology. – 2018. – Vol. 1. – P. 1–10.
36. Jacoby R., Peukert M., Succurro A., Koprivova A., Kopriva S. The role of soil microorganisms in plant mineral nutrition – Current knowledge and future directions // Frontiers in Plant Science. – 2017. – Vol. 8. – Article 1617.
37. Leake J., Johnson D., Donnelly D., Muckle G., Boddy L., Read D. Erratum: Networks of power and influence: the role of mycorrhizal mycelium in controlling plant communities and agroecosystem functioning // Canadian Journal of Botany. – 2004. – Vol. 82. – P. 1016–1045.
38. Leski T., Aučina A., Skridaila A. Ectomycorrhizal community structure of different genotypes of Scots pine under forest nursery conditions // Mycorrhiza. – 2010. – Vol. 20. – P. 473–481.
39. Lu N., Zhou X., Cui M., Yu M., Zhou J. X., Qin Y. S., Li Y. Colonization with arbuscular mycorrhizal fungi promotes the growth of Morus alba L. seedlings under greenhouse conditions // Forests. – 2015. – Vol. 6. – P. 734–747.
40. Lu N., Yu M., Cui M., Luo Z., Feng Y., Cao S., Sun Y., Li Y. Effects of different ectomycorrhizal fungal inoculates on the growth of Pinus tabulaeformis seedlings under greenhouse conditions // Forests. – 2016. – Vol. 7. – Article 316.
41. Luo S., Phillips R. P., Jo I., Fei S., Liang J., Schmid B., Eisenhauer N. Higher productivity in forests with mixed mycorrhizal strategies // Nature Communications. – 2023. – Vol. 14. – Article 1377.
42. Ma X. C., Geng Q. H., Zhang H. G., Bian C. Y., Chen H. Y. H., Jiang D. L., Xu X. Global negative effects of nutrient enrichment on arbuscular mycorrhizal fungi, plant diversity and ecosystem multifunctionality // New Phytologist. – 2021. – Vol. 229. – P. 2957–2969.
43. Martin Francis M., Uroz Stéphane, Barker David G. Ancestral alliances: Plant mutualistic symbioses with fungi and bacteria // Science. – 2017. - Vol. 356. - Article 819.
44. Marx D. H., Marrs L. F., Cordell C. E. Practical use of the mycorrhizal fungal technology in forestry, reclamation, arboriculture, agriculture, and horticulture // Dendrobiology. – 2002. – Vol. 47. – P. 27–40.
45. Meddad-Hamza A., Beddiar A., Gollotte A., Lemoine M. C., Kuszala C., Gianinazzi S. Arbuscular mycorrhizal fungi improve the growth of olive trees and their resistance to transplantation stress // African Journal of Biotechnology. – 2010. – Vol. 9. – P. 1159–1167.
46. Miller R. M., Wilson G. W. T., Johnson N. C. Arbuscular mycorrhizae and grassland ecosystems // In: Southworth D. (ed.) Biocomplexity of Plant–Fungal Interactions. – Wiley, 2012. – P. 59–84.
47. Nicolas C., Martin-Bertelsen T., Floudas D., Bentzer J., Smits M., Johansson T., Troein C., Persson P., Tunlid A. The soil organic matter decomposition mechanisms in ectomycorrhizal fungi are tuned for liberating soil organic nitrogen // ISME Journal. – 2019. – Vol. 13. – P. 977–988.
48. Orwin K. H., Dickie I. A., Wood J. R., Bonner K. I., Holdaway R. J. Soil microbial community structure explains the resistance of respiration to a dry–rewet cycle, but not soil functioning under static conditions // Functional Ecology. – 2016. – Vol. 30. – P. 1430–1439.
49. Priyashantha A. K. H., Dai D. Q., Bhat D. J., Stephenson S. L., Promputtha I., Kaushik P., Tibpromma S., Karunarathna S. C. Plant–fungi interactions: where it goes? // Biology. – 2023. – Vol. 12. – Article 809.
50. Quoreshi A. M., Khasa D. P. Effectiveness of mycorrhizal inoculation in the nursery on root colonization, growth, and nutrient uptake of aspen and balsam poplar // Biomass and Bioenergy. – 2008. – Vol. 32. – P. 381–391.
51. Rillig M. C., Aguilar-Trigueros C. A., Bergmann J., Verbruggen E., Veresoglou S. D., Lehmann A. Plant root and mycorrhizal fungal traits for understanding soil aggregation // New Phytologist. – 2015. – Vol. 205. – P. 1385–1398. – DOIhttps://doi.org/10.1111/nph.13045.
52. Rocha I., Ma Y., Souza-Alonso P., Vosatka M., Freitas H., Oliveira R. S. Seed coating: a tool for delivering beneficial microbes to agricultural crops // Frontiers in Plant Science. – 2019. – Vol. 10. – Article 1357.
53. Smith S. E., Read D. J. Mycorrhizal Symbiosis. – 3rd ed. – London : Academic Press, 2008.
54. Song Y. Y., Simard S. W., Carroll A., Mohn W. W., Zeng R. S. Defoliation of interior Douglas-fir elicits carbon transfer and stress signalling to ponderosa pine neighbors through ectomycorrhizal networks // Scientific Reports. – 2015. – Vol. 5. – P. 1–9.
55. Staddon P. L., Ramsey C. B., Ostle N., Ineson P., Fitter A. H. Rapid turnover of hyphae of mycorrhizal fungi determined by AMS microanalysis of 14C // Science. – 2003. – Vol. 300. – P. 1138–1140.
56. Tedersoo L., Smith M. E. Lineages of ectomycorrhizal fungi revisited: foraging strategies and novel lineages revealed by sequences from belowground // Fungal Biology Reviews. – 2013. – Vol. 27. – P. 83–99.
57. Teste F. P., Simard S. W. Mycorrhizal networks and distance from mature trees alter patterns of competition and facilitation in dry Douglas-fir forests // Oecologia. – 2008. – Vol. 158. – P. 193–203.
58. Torti S. D., Coley P. D., Kursar T. A. Causes and consequences of monodominance in tropical lowland forests // The American Naturalist. – 2001. – Vol. 157. – P. 141–153.
59. Van der Heijden M. G. A., Martin F. M., Selosse M. A., Sanders I. R. Mycorrhizal ecology and evolution: the past, the present, and the future // New Phytologist. – 2015. – Vol. 205. – P. 1406–1423.
60. Van der Heijden M. G. A., Streitwolf-Engel R., Riedl R., Siegrist S., Neudecker A., Ineichen K. The mycorrhizal contribution to plant productivity, plant nutrition and soil structure in experimental grassland // New Phytologist. – 2006. – Vol. 172. – P. 739–752.
61. Verbruggen E., Pena R., Fernandez C. W., Soong J. L. Mycorrhizal interactions with saprotrophs and impact on soil carbon storage // In: Mycorrhizal Mediation of Soil. – Elsevier, 2017. – P. 441–460.
62. Veresoglou S. D., Chen B. D., Rillig M. C. Arbuscular mycorrhiza and soil nitrogen cycling // Soil Biology and Biochemistry. – 2012. – Vol. 46. – P. 53–62.
63. Veresoglou S. D., Wulf M., Rillig M. C. Facilitation between woody and herbaceous plants that associate with arbuscular mycorrhizal fungi in temperate European forests // Ecology and Evolution. – 2017. – Vol. 7. – P. 1181–1189
64. Wallander H., Ekblad A. The importance of ectomycorrhizal networks for nutrient retention and carbon sequestration in forest ecosystems // In: Mycorrhizal Networks. – Springer, 2015. – P. 69–90.
65. Wang Q., Liu M., Wang Z., Li J., Liu K., Huang D. The role of arbuscular mycorrhizal symbiosis in plant abiotic stress // Frontiers in Microbiology. – 2024. – Vol. 14. – Article 1323881.
66. Wezowicz K., Rozpadek P., Turnau K. Interactions of arbuscular mycorrhizal and endophytic fungi improve seedling survival and growth in post-mining waste // Mycorrhiza. – 2017. – Vol. 27. – P. 499–511.
67. Xu H., Shi Y., Chen C., Pang Z., Zhang G., Zhang W., Kan H. Arbuscular mycorrhizal fungi selectively promoted the growth of three ecological restoration plants // Plants. – 2024. – Vol. 13, № 12. – Article 1678.
68. Yin H., Wheeler E., Phillips R. Root-induced changes in nutrient in forest depend on exudation rates // Soil Biology and Biochemistry. – 2014. – Vol. 78. – P. 213–221.
69. Zhang L., Xu M., Liu Y., Zhang F. S., Hodge A., Feng G. Carbon and phosphorus exchange may enable cooperation between an arbuscular mycorrhizal fungus and a phosphate-solubilizing bacterium // New Phytologist. – 2016. – Vol. 210. – P. 1022–1032.
