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Boron and other elements in sporophores of ectomycorrhizal and saprotrophic fungi

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Abstract

Fungi are usually thought not to have a boron (B) requirement. It is not known if mycorrhizas take up B from low concentrations that are common in forest soils, as fungi might also immobilise B. Here, we studied the B concentrations in sporophores of 49 ectomycorrhizal and 10 saprotrophic fungi to assess whether B is translocated in mycelium or not. Additionally, P and metal concentrations were measured for comparison. Variability both within species and between species was very large, as the lowest measured B concentration was 0.01 mg kg−1 in Amanita muscaria, and the highest was 280 mg kg−1 in Paxillus involutus. There was no clear difference between saprotrophic and mycorrhizal fungi. The majority of species did not accumulate B at more than 0.01–3 mg kg−1, but there were some species that consistently had median concentration values higher than 5–6 mg kg−1 and much higher maximum values, particularly Paxillus involutus, Lactarius necator and several Russula species. Most species increased their B concentration in B fertilised plots, but there were exceptions, particularly Rozites caperatus and Lactarius camphoratus. Boron concentrations did not correlate with those of other elements. In conclusion, B is translocated in the mycelia of most of the studied species. The differences between species may be due to differences in their water use, or carbohydrates used in translocation. It remains to be studied, if B concentrations in mycorrhizas or mycelia in soil are in the same order of magnitude as the larger ones found here, and if this has any effects on the host plants.

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References

  • Aphalo PJ, Schoettle AW, Lehto T (2002) Leaf life span and the mobility of non-mobile” mineral nutrients—the case of boron in conifers. Silva Fenn 36:671–680

    Google Scholar 

  • Berthelsen BO, Olsen RA, Steinnes E (1995) Ectomycorrhizal heavy metal accumulation as a contributing factor to heavy metal levels in organic surface soils. Sci Total Environ 170:141–149

    Article  CAS  Google Scholar 

  • Brown PH, Shelp BJ (1997) Boron mobility in plants. Plant Soil 193:85–101

    Article  CAS  Google Scholar 

  • Cajander AK (1949) Forest types and their significance. Acta For Fenn 56:1–71

    Google Scholar 

  • Chudzynski K, Falandysz J (2008) Multivariate analysis of elements content of Larch Bolete (Suillus grevillei) mushroom. Chemosphere 73:1230–1239

    Article  PubMed  CAS  Google Scholar 

  • Dannel F, Pfeffer H, Römheld V (2002) Update on boron in higher plants–uptake, primary translocation and compartmentation. Plant Biol 4:193–204

    Article  CAS  Google Scholar 

  • Dordas C, Brown PH (2001) Evidence for channel mediated transport of boric acid in squash (Cucurbita pepo). Plant Soil 235:95–103

    Article  CAS  Google Scholar 

  • Fitzpatrick KL, Reid RJ (2009) The involvement of aquaglyceroporins in transport of boron in barley roots. Plant Cell Environ 32:1357–1365

    Article  PubMed  CAS  Google Scholar 

  • Goldbach HE, Wimmer MA (2007) Boron in plants and animals: Is there a role beyond cell-wall structure? J Plant Nutr Soil Sci 170:39–48

    Article  CAS  Google Scholar 

  • Halonen O, Tulkki H, Derome J (1983) Nutrient analysis methods. Finnish For Res Inst Res Notes 121:1–28

    Google Scholar 

  • Hansen I, Knudsen H (1992) Nordic Macromycetes Vol 2, Polyporales, Boletales, Agaricales, Russulales. Nordsvamp, Helsinki. 474pp

  • Hedh J, Johansson T, Tunlid A (2009) Variation in host specificity and gene content in strains from genetically isolated lineages of the ectomycorrhizal fungus Paxillus involutus s. lat. Mycorrhiza 19:549–558

    Article  PubMed  Google Scholar 

  • Högberg MN, Högberg P (2002) Extramatrical ectomycorrhizal mycelium contributes one third of microbial biomass and produces, together with associated roots, half the dissolved organic carbon in a forest soil. New Phytol 154:791–795

    Article  Google Scholar 

  • Hu H, Brown PH (1997) Absorption of boron by plant roots. Plant Soil 193:49–58

    Article  CAS  Google Scholar 

  • Hu H, Penn SG, Lebrilla CB, Brown PH (1997) Isolation and characterization of soluble boron complexes in higher plants. The mechanism of phloem mobility of boron. Plant Physiol 113:649–655

    Article  PubMed  CAS  Google Scholar 

  • Kaya A, Karakaya HC, Fomenko DE, Gladyshev VN, Koc A (2009) Identification of a novel system for B transport: Atr1 is a main boron exporter in yeast. Molecular and Cellular Biology: 3665–3674

  • Lehto T (1995) Boron retention in limed forest mor. Forest Ecol Manage 78:11–20

    Article  Google Scholar 

  • Lehto T, Mälkönen E (1994) Effects of liming and boron fertilization on boron uptake of Picea abies. Plant Soil 163:55–64

    CAS  Google Scholar 

  • Lehto T, Lavola A, Kallio E, Aphalo PJ (2004a) Boron uptake by ectomycorrhizas of silver birch. Mycorrhiza 14:209–212

    Article  PubMed  CAS  Google Scholar 

  • Lehto T, Lavola A, Julkunen-Tiitto R, Aphalo PJ (2004b) Boron retranslocation in Scots pine and Norway spruce. Tree Physiol 24:1011–1017

    PubMed  CAS  Google Scholar 

  • Lehto T, Räisänen M, Lavola A, Julkunen-Tiitto APJ (2004c) Boron mobility in deciduous forest trees in relation to their polyols. New Phytol 163:333–339

    Article  CAS  Google Scholar 

  • Lewis DH (1980) Boron, lignification and the origin of vascular plants—a unified hypothesis. New Phytol 84:209–229

    Article  CAS  Google Scholar 

  • Lilleskov EA, Bruns TD, Dawson TE, Camacho FJ (2009) Water sources and controls on water-loss rates of epigeous ectomycorrhizal fungal sporophores during summer drought. New Phytol 182:483–494

    Article  PubMed  Google Scholar 

  • Marschner H (1995) Mineral nutrition of higher plants. Academic Press

  • Martin F, Nehls U (2009) Harnessing ectomycorrhizal genomics for ecological insights. 12: 508–515

  • Michael G, Marschner H (1962) Einfluss unterschiedlicher Luftfeuchtigkeit und Transpiration auf Mineralstoffaufnahme und–Verteilung Z Pflanzenernähr Düng Bodenk 96: 200–212

    Google Scholar 

  • Möttönen M, Lehto T, Aphalo PJ, Kukkola M, Mälkönen E (2003) Response of mature stands of Norway spruce (Picea abies) to boron fertilization. For Ecol Manage 180:401–412

    Article  Google Scholar 

  • Möttönen M, Lehto T, Rita H, Aphalo PJ (2005) Recovery of Norway spruce (Picea abies) seedlings from repeated drought as affected by boron nutrition. Trees 19:213–223

    Article  Google Scholar 

  • Nehls U (2008) Mastering ectomycorrhizal symbiosis: the impact of carbohydrates. J Exp Bot 59:1097–1108

    Article  PubMed  CAS  Google Scholar 

  • Ohtonen R (1982) Mineral concentrations in some edible fungi and their relation to fruit-body size and mineral status of substrate. Ann Bot Fennici 19:203–209

    CAS  Google Scholar 

  • Räisänen M, Repo T, Lehto T (2009) Cold acclimation of Norway spruce roots and shoots after boron fertilization. Silva Fenn 43:223–233

    Google Scholar 

  • Shi L, Guttenberger M, Kottke I, Hampp R (2002) The effect of drought on mycorrhizas of beech (Fagus sylvatica L): changes in community structure, and the content of carbohydrates and nitrogen storage bodies of the fungi. Mycorrhiza 12:303–311

    Article  PubMed  CAS  Google Scholar 

  • Smith SE, Read DJ (2008) Mycorrhizal symbiosis. Academic Press

  • Sutinen S, Vuorinen M, Rikala R (2006) Developmental disorders in buds and needles of mature Norway spruce, Picea abies (L.) Karst, in relation to needle boron concentrations. Trees 20:559–570

    Article  CAS  Google Scholar 

  • Tanaka M, Fujiwara T (2008) Physiological roles and transport mechanisms of boron: perspectives from plants. Eur J Physiol 456:671–677

    Article  CAS  Google Scholar 

  • Tibbett M, Sanders FE, Cairney JWG (2002) Low-temperature-induced changes in trehalose, mannitol and arabitol associated with enhanced tolerance to freezing in ectomycorrhizal basidiomycetes (Hebeloma spp.). Mycorrhiza 12:249–255

    Article  PubMed  CAS  Google Scholar 

  • Tyler G (1980) Metals in sporophores of Basidiomycetes. Trans Brit Mycol Soc 74:41–49

    Article  CAS  Google Scholar 

  • Tyler G (2005) Changes in the concentrations of major, minor and rare-earth elements during leaf senescence and decomposition in a Fagus sylvatica forest. Forest Ecol Manage 206:167–177

    Article  Google Scholar 

  • Wallander H, Nilsson LO, Hagerberg D, Bååth E (2001) Estimation of the biomass and seasonal growth of external mycelium of ectomycorrhizal fungi in the field. New Phytol 151:753–760

    Article  CAS  Google Scholar 

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Acknowledgements

We thank Germund Tyler for kindly informing us about the data on B concentrations in sporophores that were inadvertently left out from his paper (Tyler 2005). We thank Aino Rummukainen and Mikko Räisänen for help in the field, and Merja Essell and Rauni Oksman in the laboratory. The study was supported by the Foundation for Research of Natural Resources in Finland, and at the reporting stage, the Academy of Finland, decision n:o 123637.

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Correspondence to Tarja Lehto.

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Lavola, A., Aphalo, P.J. & Lehto, T. Boron and other elements in sporophores of ectomycorrhizal and saprotrophic fungi. Mycorrhiza 21, 155–165 (2011). https://doi.org/10.1007/s00572-010-0321-7

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