, Volume 86, Issue 6, pp 786–792 | Cite as

Yeast population of the Kindo Peninsula lichens

  • A. V. Kachalkin
  • A. M. Glushakova
  • T. A. Pankratov
Experimental Articles


Yeast abundance and species diversity in the lichens collected at the Kindo Peninsula (Karelia) were studied. A total of 14 lichen species analyzed belonged to the genera Bryoria, Cladonia, Hypogymnia, Icmadophila, Nephroma, Peltigera, and Ramalina. Abundance of cultured yeasts in lichens was intermediate between soil and phyllosphere. The average yeast number on lichens was ~2.5 × 103 CFU/g, while it exceeded 8 × 103 CFU/g on plants and reached only 1 × 103 CFU/g in soil. Yeast population of different parts of Cladonia lichens was found to vary significantly in abundance, species diversity, and community structure. The highest yeast abundance and diversity were revealed in the growth zone. Fifteen yeast species were isolated from lichens, including 6 basidiomycetous and 9 ascomycetous ones. Unlike soils and plants, yeast population of lichens consisted mainly of ascomycetous species, with predominance of Candida sphagnicola and anamorphous yeasts of the genus Dothiora. These results show that yeasts from different taxonomic and ecological groups are a necessary component of lichens; conditions favoring the preservation and development of specific yeast communities differing from the typical soil and phyllosphere yeast complexes are formed in the lichens of northern taiga forests.


yeasts lichens lichenosphere Subarctic areas MSU White Sea Biological Station Cladonia Dothiora 


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  1. Açikgöz, B., Karalti, I., Ersöz, M., Coşkun, Z.M., Cobanoğlu, G., and Sesal, C., Screening of antimicrobial activity and cytotoxic effects of two Cladonia species, Z. Naturforsch. C, 2013, vol. 68, nos. 5−6, pp. 191–197.CrossRefPubMedGoogle Scholar
  2. Alam, Md.A., Gauslaa, Y., and Solhaug, K.A., Soluble carbohydrates and relative growth rates in chloro-, cyano-, and cephalolichens: effects of temperature and nocturnal hydration, New Phytol., 2015, vol. 208, no. 3, pp. 750–762.CrossRefPubMedGoogle Scholar
  3. Andreev, V.N., Growth of fodder lichens and approaches to its regulation, Trudy BIN AN SSSR, Ser. 3, Geobotany, 1954, no. 9, pp. 11–74.Google Scholar
  4. Babjeva, I. and Reshetova, I., Yeast resources in natural habitats at polar circle latitude, Food Technol. Biotechnol., 1998, vol. 36, pp. 1–5.Google Scholar
  5. Chernov, I.Yu., Ecology of yeasts of Taimyr tundra, Cand. Sci. (Biol.) Dissertation, Moscow, Mos. Gos. Univ., 1984.Google Scholar
  6. Connell, L.B., Rodriguez, R.R., Redman, R.S., and Dalluge, J.J., Cold-adapted yeasts in Antarctic deserts, in Cold-Adapted Yeasts, Buzzini, P. and Margesin, R., Eds., Springer, 2014, pp. 75–98.CrossRefGoogle Scholar
  7. Elix, J.A. and Stocker-Wörgötter, A., Biochemistry and secondary metabolites, in Lichen Biology, 2nd ed., Nash, Th.H., III, Ed., New York: Cambridge Univ. Press, 2008, pp. 104–106.CrossRefGoogle Scholar
  8. Fonseca, Á. and Inácio, J., Phylloplane yeasts, in Biodiversity and Ecophysiology of Yeasts, Rosa, C. and Gábor, P., Eds., 2006, pp. 263–303.CrossRefGoogle Scholar
  9. Glushakova, A.M. and Chernov, I.Yu., Seasonal dynamic of the numbers of epiphytic yeasts, Microbiology (Moscow), 2007, vol. 76, no. 5, pp. 590–595.CrossRefGoogle Scholar
  10. Glushakova, A.M., Kachalkin, A.V., Maksimova, I.A., and Chernov, I.Yu., Yeasts in Hevea brasiliensis latex, Microbiology (Moscow), 2016, vol. 85, no. 4, pp. 488–492.CrossRefGoogle Scholar
  11. Hawksworth, D.L. and Honegger, R., The lichen thallus: a symbiotic phenotype of nutritionally specialized fungi and its response to gall producers, in Plant Galls: Organisms, Interactions, Populations, Williams, M.A.J., Ed., Oxford: Clarendon, 1994, pp. 77–98.Google Scholar
  12. Kachalkin, A.V., Glushakova, A.M., Yurkov, A.M., and Chernov, I.Yu., Characterization of yeast groupings in the phyllosphere of sphagnum mosses, Microbiology (Moscow), 2008, vol. 77, no. 4, pp. 474–481.CrossRefGoogle Scholar
  13. Kachalkin, A.V. and Yurkov, A.M., Yeast communities in Sphagnum phyllosphere along the temperature-moisture ecocline in the boreal forest-swamp ecosystem and description of Candida sphagnicola sp. nov., Antonie van Leeuwenhoek, 2012, vol. 102, no. 1, pp. 29–43.CrossRefPubMedGoogle Scholar
  14. Kachalkin, A.V., Yeasts of the White Sea intertidal zone and description of Glaciozyma litorale sp. nov., Antonie van Leeuwenhoek, 2014, vol. 105, no. 6, pp. 1073–1083.CrossRefPubMedGoogle Scholar
  15. Katalog bioty Belomorskoi biologicheskoi stantsii MGU (Catalogue of Biota of the MSU White Sea Biological Station), Chesunov, A.V., Kalyakina, N.M., and Bubnova, E.N., Eds., Moscow: KMK, 2008.Google Scholar
  16. Larson, D.W., The absorption and release of water by lichens, Bibliotheca Lichenologica, 1987, vol. 25, pp. 351–360.Google Scholar
  17. Pandey, A., Mishra, R.K., Tiwari, A.K., Kumar, A., Bajaj, A.K., and Dikshit, A., Management of cosmetic embarrassment caused by Malassezia spp. with fruticose lichen Cladia using phylogenetic approach, BioMed. Research International, 2013, Article ID 169794, pp. 1–8.Google Scholar
  18. Pankratov, T.A., Kachalkin, A.V., Korchikov, E.S., and Dobrovol’skaya, T.G., Microbial communities of lichens, Microbiology (Moscow), 2017, vol. 86, no. 3, pp. 293–309.CrossRefGoogle Scholar
  19. Santiago, I.F., Soares, M.A., Rosa, C.A., and Rosa, L.H., Lichensphere: a protected natural microhabitat of the nonlichenised fungal communities living in extreme environments of Antarctica, Extremophiles, 2015, vol. 19, no. 6, pp. 1087–1097.CrossRefPubMedGoogle Scholar
  20. Schoch, C.L., Crous, P.W., Groenewald, J.Z., Boehm, E.W., Burgess, T.I., de Gruyter, J., de Hoog, G.S., Dixon, L.J., Grube M., Gueidan, C., Harada, Y., Hatakeyama, S., Hirayama, K., Hosoya, T., Huhndorf, S.M., et al., A class-wide phylogenetic assessment of Dothideomycetes, Stud. Mycol. 2009, vol. 64, pp. 1–15.CrossRefPubMedPubMedCentralGoogle Scholar
  21. Spribille, T., Tuovinen, V., Resl, P., Vanderpool, D., Wolinski, H., Aime, M.C., Schneider, K., Stabentheiner, E., Toome-Heller, M., Thor, G., Mayrhofer, H., Johannesson, H., and McCutcheon, J.P., Basidiomycete yeasts in the cortex of ascomycete macrolichens, Science, 2016, vol. 353, no. 6298, pp. 488–492.CrossRefPubMedGoogle Scholar
  22. Streletskii, R.A., Kachalkin, A.V., Glushakova, A.M., Demin, V.V., and Chernov I.Yu., Quantitative determination of indole-3-acetic acid in yeasts using high performance liquid chromatography−tandem mass spectrometry, Microbiology (Moscow), 2016, vol. 85, no. 6, pp. 727–736.CrossRefGoogle Scholar
  23. Vishniac, H.S., Yeast biodiversity in the Antarctic, in The Yeast Handbook. Biodiversity and Ecophysiology of Yeasts, Peter, G. and Rosa, C., Eds., Berlin: Springer, 2006, pp. 419–440.CrossRefGoogle Scholar
  24. Vu, D., Groenewald, M., Szöke, S., Cardinali, G., Eberhardt, U., Stielow, B., de Vries, M., Verkleij, G.J., Crous, P.W., Boekhout, T., and Robert, V., DNA barcoding analysis of more than 9000 yeast isolates contributes to quantitative thresholds for yeast species and genera delimitation, Stud. Mycol., 2016, vol. 85, pp. 91–105.CrossRefPubMedPubMedCentralGoogle Scholar
  25. Woranovicz-Barreira, S.M., Gorin, P.A.J., Sassaki, G.L., Tischer, C.A., Ahti, T., and Iacomini, M., Chemotyping glucans from lichens of the genus Cladonia, Phytochemistry, 1999, vol. 52, pp. 1069–1074.CrossRefGoogle Scholar
  26. Zalar, P. and Gunde-Cimerman N., Cold-adapted yeasts in Arctic habitats, in Cold-Adapted Yeasts, Buzzini, P. and Margesin, R., Eds., Springer, 2014, pp. 49–75.CrossRefGoogle Scholar
  27. Zelenskaya, T.G., Eremenko, R.S., and Stepanenko, E.E., Investigation of anthropogenic load in an industrial city of Stavropol by lichenoindexation, Usp. Sovr. Estestvozn., 2012, no. 2, pp. 20–21.Google Scholar

Copyright information

© Pleiades Publishing, Ltd. 2017

Authors and Affiliations

  • A. V. Kachalkin
    • 1
  • A. M. Glushakova
    • 1
  • T. A. Pankratov
    • 1
  1. 1.Lomonosov Moscow State UniversityMoscowRussia

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