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Abundance, richness, and succession of microfungi in relation to chemical changes in Antarctic moss profiles

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Abstract

Little is known in continental Antarctic about patterns of abundance, diversity, and succession of microfungi within moss profiles consisting of live, senescent, and dead tissues in different stages of decomposition. In the present study, vertical patterns of the abundance and diversity of microfungi and their relationship with chemical compositions were examined within moss colonies collected from coastal outcrops in the Lützow–Holm Bay area (Queen Maud Land), East continental Antarctica. Total and darkly pigmented hyphal length, the richness of molecular operational taxonomic units (MOTUs) of microfungi, and the occurrence of Phoma herbarum and Pseudogymnoascus pannorum increased with the depth of moss profiles. The content of organic chemical components and nitrogen in moss tissues decreased, whereas ash content increased with the depth of moss profiles. Relative amount of recalcitrant compounds and total carbohydrates did not significantly differ among the vertical layers. The downward increase of the microfungal richness and occurrence in the Antarctic moss profiles without MOTU replacement was consistent with the directional-nonreplacement model of succession, indicative of the high environmental resistance, which represents the sum of the adverse factors hindering the success of species establishment. This contrasted with the fungal succession in arctic moss profiles, which accorded with the directional-replacement model, in which species replacement took place due to modification of habitat and competition. More hostile environmental conditions than those in the Arctic characterized the fungal succession and limited the fungal decomposition of moss in continental Antarctica.

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References

  • Altschul SF, Madden TL, Schaffer AA, Zhang JH, Zhang Z, Miller W, Lipman DJ (1997) Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res 25:3389–3402

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Arenz BE, Blanchette RA, Farrell RL (2014) Fungal diversity in Antarctic soils. In: Cowan DA (ed) Antarctic terrestrial microbiology. Springer, Berlin, pp 35–53

    Chapter  Google Scholar 

  • Bailey AD, Wynn-Williams DD (1982) Soil microbiological studies at Signy Island, South Orkney Islands. Br Antarct Surv Bull 51:167–191

    Google Scholar 

  • Baker JH (1972) The rate of production and decomposition of Chorisodontium aciphyllum (Hook. f. & Wils.) Broth. Br Antarct Surv Bull 27:123–129

    Google Scholar 

  • Berg B (1986) Nutrient release from litter and humus in coniferous forest soils—a mini review. Scand J For Res 1:359–369

    Article  Google Scholar 

  • Berg B, Söderström B (1979) Fungal biomass and nitrogen in decomposing Scots pine needle litter. Soil Biol Biochem 11:339–341

    Article  CAS  Google Scholar 

  • Bridge PD, Newsham KK (2009) Soil fungal community composition at Mars Oasis, a southern maritime Antarctic site, assessed by PCR amplification and cloning. Fungal Ecol 2:66–74

    Article  Google Scholar 

  • Butler MJ, Day AW (1998) Fungal melanins: a review. Can J Microbiol 44:1115–1136

    Article  CAS  Google Scholar 

  • Cannone N, Convey P, Guglielmin M (2013) Diversity trends of bryophytes in continental Antarctica. Polar Biol 36:259–271

    Article  Google Scholar 

  • Davey ML, Currah RS (2006) Interactions between mosses (Bryophyta) and fungi. Can J Bot 84:1509–1519

    Article  Google Scholar 

  • Davis RC (1981) Structure and function of two Antarctic terrestrial moss communities. Ecol Monogr 51:125–143

    Article  Google Scholar 

  • Domsch KH, Gams W, Anderson TH (2007) Compendium of soil fungi, 2nd edn. IHW-Verlag, Eching

    Google Scholar 

  • Dowding P, Widden P (1974) Some relationships between fungi and their environment in tundra regions. In: Holding AJ, Heal OW, MacLean SF Jr, Flangan PW (eds) Soil organisms and decomposition in tundra. University of Alaska, Tundra Biome Steering Committee, Fairbanks, pp 123–150

    Google Scholar 

  • Dubois M, Gilles KA, Hamilton JK, Rebers PA, Smith E (1956) Colorimetric method for determination of sugars and related substances. Anal Chem 28:350–356

    Article  CAS  Google Scholar 

  • Erickson M, Miksche GE (1974) On the occurrence of lignin or polyphenols in some mosses and liverworts. Phytochemistry 13:2295–2299

    Article  CAS  Google Scholar 

  • Fenton JHC (1980) The rate of peat accumulation in Antarctic moss banks. J Ecol 68:211–228

    Article  Google Scholar 

  • Fernandez CW, Koide RT (2014) Initial melanin and nitrogen concentrations control the decomposition of ectomycorrhizal fungal litter. Soil Biol Biochem 77:150–157

    Article  CAS  Google Scholar 

  • Fukasawa Y, Osono T, Takeda H (2009) Effects of attack of saprobic fungi on twig litter decomposition by endophytic fungi. Ecol Res 24:1067–1073

    Article  Google Scholar 

  • Gardes M, Bruns TD (1993) ITS primer with enhanced specificity for basidiomycetes: application to the identification of mycorrhizae and rust. Mol Ecol 21:113–118

    Article  Google Scholar 

  • Hirose D, Tanabe Y, Uchida M, Kudoh S, Osono T (2013) Microfungi associated with withering willow wood in ground contact near Syowa Station, East Antarctica for 40 years. Polar Biol 36:919–924

    Article  Google Scholar 

  • Hirose D, Hobara S, Matsuoka S, Kato K, Tanabe Y, Uchida M, Kudoh S, Osono T (2016) Diversity and community assembly of moss-associated fungi in ice-free coastal outcrops of continental Antarctica. Fungal Ecol 24:94–101

    Article  Google Scholar 

  • Jones PCT, Mollison JE (1948) A technique for the quantitative estimation of soil microorganisms. J Gen Microbiol 2:54–69

    Article  CAS  Google Scholar 

  • Kanda H, Inoue M (1994) Ecological Monitoring of moss and lichen vegetation in the Syowa station area, Antarctica. Proc NIPR Symp Polar Biol 7:221–231

    Google Scholar 

  • King HGC, Heath GW (1967) The chemical analysis of small samples of leaf material and the relationship between the disappearance and composition of leaves. Pedobiologia 7:192–197

    Google Scholar 

  • Lehtonen MT, Akita M, Kalkkinen N, Ahola-Iivarinen E, Rönnholm G, Somervuo P, Thelander M, Valkonen JPT (2009) Quickly-released peroxidase of moss in defense against fungal invaders. New Phytol 183:432–443

    Article  CAS  PubMed  Google Scholar 

  • Leung GL, Robson GD, Robinson CH (2011) Characterisation of cold-tolerant fungi from a decomposing High Arctic moss. Soil Biol Biochem 43:1975–1979

    Article  CAS  Google Scholar 

  • Lindo Z, Gonzalez A (2010) The Bryosphere: an integral and influential component of the Earth’s biosphere. Ecosystems 13:612–627

    Article  Google Scholar 

  • Malosso E, Waite IS, English L, Hopkins DW, O’Donnell AG (2006) Fungal diversity in maritime Antarctic soils determined using a combination of culture isolation, molecular fingerprinting and cloning techniques. Polar Biol 29:552–561

    Article  Google Scholar 

  • McRae CF, Seppelt RD (1999) Filamentous fungi of the Windmill Islands, continental Antarctica. Effect of water content in moss turves on fungal diversity. Polar Biol 22:389–394

    Article  Google Scholar 

  • Miller OK Jr, Laursen GA (1974) Belowground fungal biomass on US tundra biome sites at Barrow, Alaska. In: Holding AJ, Heal OW, MacLean SF Jr, Flangan PW (eds) Soil organisms and decomposition in tundra. University of Alaska, Tundra Biome Steering Committee, Fairbanks, pp 151–158

    Google Scholar 

  • Ochyra R, Lewis-Smith RI, Bednarek-Ochyra H (2008) The illustrated moss flora of Antarctica. Cambridge University Press, Cambridge

    Google Scholar 

  • Osono T, Takeda H (2001) Organic chemical and nutrient dynamics in decomposing beech leaf litter in relation to fungal ingrowth and succession during three year decomposition processes in a cool temperate deciduous forest in Japan. Ecol Res 16:649–670

    Article  CAS  Google Scholar 

  • Osono T, Takeda H (2004) Accumulation and release of nitrogen and phosphorus in relation to lignin decomposition in leaf litter of 14 tree species in a cool temperate forest. Ecol Res 19:593–602

    Article  Google Scholar 

  • Osono T, Takeda H (2005) Limit values for decomposition and convergence process of lignocellulose fraction in decomposing leaf litter of 14 tree species in a cool temperate forest. Ecol Res 20:51–58

    Article  CAS  Google Scholar 

  • Osono T, Trofymow JA (2012) Microfungal diversity associated with Kindbergia oregana in successional forests of British Columbia. Ecol Res 27:35–41

    Article  Google Scholar 

  • Osono T, Hobara S, Koba K, Kameda K (2006a) Reduction of fungal growth and lignin decomposition in needle litter by avian excreta. Soil Biol Biochem 38:1623–1630

    Article  CAS  Google Scholar 

  • Osono T, Hirose D, Fujimaki R (2006b) Fungal colonization as affected by litter depth and decomposition stage of needle litter. Soil Biol Biochem 38:2743–2752

    Article  CAS  Google Scholar 

  • Osono T, Ishii Y, Hirose D (2008) Fungal colonization and decomposition of Castanopsis sieboldii leaf litter in a subtropical forest. Ecol Res 23:909–917

    Article  Google Scholar 

  • Osono T, Hobara S, Hishinuma T, Azuma JI (2011) Selective lignin decomposition and nitrogen mineralization in forest litter colonized by Clitocybe sp. Eur J Soil Biol 47:114–121

    Article  CAS  Google Scholar 

  • Osono T, Ueno T, Uchida M, Kanda H (2012) Abundance and diversity of fungi in relation to chemical changes in arctic moss profiles. Polar Sci 6:121–131

    Article  Google Scholar 

  • Osono T, Matsuoka S, Hirose D, Uchida M, Kanda H (2014) Fungal colonization and decomposition of leaves and stems of Salix arctica on deglaciated moraines in high-Arctic Canada. Polar Sci 8:207–216

    Article  Google Scholar 

  • Preston CM, Trofymow JA, Sayer BG, Niu J (1997) 13C nuclear magnetic resonance spectroscopy with cross-polarization and magic-angle spinning investigation of the proximate-analysis fractions used to assess litter quality in decomposition studies. Can J Bot 75:1601–1613

    Article  CAS  Google Scholar 

  • Rao S, Chan Y, Lacap DC, Hyde KD, Pointing SB, Farrell RL (2012) Low-diversity fungal assemblage in an Antarctic Dry Valleys soil. Polar Biol 35:567–574

    Article  Google Scholar 

  • Robinson CH (2001) Cold adaptation in Arctic and Antarctic fungi. New Phytol 151:341–353

    Article  CAS  Google Scholar 

  • Robinson CH, Borisova OB, Callaghan TV, Lee JA (1996) Fungal hyphal length in litter of Dryas octopetala in a high-Arctic polar semi-desert, Svalbard. Polar Biol 16:71–74

    Article  Google Scholar 

  • Ruisi S, Barreca D, Selbmann L, Zucconi L, Onofri S (2007) Fungi in Antarctica. Rev Environ Sci Biotechnol 6:127–141

    Article  Google Scholar 

  • Selbmann L, Onofri S, Fenice M, Federici F, Petruccioli M (2002) Production and structural characterization of the exopolysaccharide of the Antarctic fungus Phoma herbarum CCFEE 5080. Res Microbiol 153:585–592

    Article  CAS  PubMed  Google Scholar 

  • Stevens MI, Hunger SA, Hills SFK, Gemmill CEC (2007) Phantom hitch-hikers mislead estimates of genetic variation in Antarctic mosses. Plant Syst Evol 263:191–201

    Article  Google Scholar 

  • Svoboda J, Henry GHR (1987) Succession in marginal arctic environments. Arc Alp Res 19:373–384

    Article  Google Scholar 

  • Tanabe Y, Yasui S, Osono T, Uchida M, Kudoh S, Yamamuro M (2017) Abundant deposits of nutrients inside lakebeds of Antarctic oligotrophic lakes. Polar Biol 40:603–613

    Article  Google Scholar 

  • Tateno O, Hirose D, Osono T, Takeda H (2015) Beech cupules share endophytic fungi with leaves and twigs. Mycoscience 56:252–256

    Article  Google Scholar 

  • Thormann MN, Currah RS, Bayley SE (2004) Patterns of distribution of microfungi in decomposing bog and fen plants. Can J Bot 82:710–720

    Article  Google Scholar 

  • Tosi S, Casado B, Gerdol R, Caretta G (2002) Fungi isolated from Antarctic mosses. Polar Biol 25:262–268

    Google Scholar 

  • Tosi S, Onofri S, Brusoni M, Zucconi L, Vishniac H (2005) Response of Antarctic soil fungal assemblages to experimental warming and reduction of UV radiation. Polar Biol 28:470–482

    Article  Google Scholar 

  • Vilgalys R, Hester M (1990) Rapid genetic identification and mapping of enzymatically amplified ribosomal DNA from several Cryptococcus species. J Bacteriol 172:4238–4246

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Yu NH, Kim JA, Jeong MH, Cheong YH, Hong SG, Jung JS, Koh YJ, Hur JS (2014) Diversity of endophytic fungi associated with bryophyte in the maritime Antarctic (King George Island). Polar Biol 37:27–36

    Article  CAS  Google Scholar 

  • Zhang T, Zhang YQ, Liu HY, Wei YZ, Li HL, Su J, Zhao LX, Yu LY (2013) Diversity and cold adaptation of culturable endophytic fungi from bryophytes in the Fildes Region, King George Island, maritime Antarctica. FEMS Microb Ecol 341:52–61

    Article  CAS  Google Scholar 

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Acknowledgements

We thank Dr. Y. Motoyoshi and members of JARE-51 for their assistance during the expedition; Dr. H. Kanda and Dr. A.S. Mori for useful discussions; Dr. K. Kato for helpful identification of moss species; and Dr. Elizabeth Nakajima for critical reading of the manuscript. This study was partially supported by the National Institute of Polar Research through General Collaboration Projects No. 26-28 to T.O. and by a Japan Society for the Promotion of Science KAKENHI Grant (No. 70370096 to M.U.).

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Correspondence to Takashi Osono.

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Hirose, D., Hobara, S., Tanabe, Y. et al. Abundance, richness, and succession of microfungi in relation to chemical changes in Antarctic moss profiles. Polar Biol 40, 2457–2468 (2017). https://doi.org/10.1007/s00300-017-2157-5

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  • DOI: https://doi.org/10.1007/s00300-017-2157-5

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