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Recent 14C-labelled assimilate allocation to Scots pine seedling root and mycorrhizosphere compartments developed on reconstructed podzol humus, E- and B- mineral horizons

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Abstract

In northern boreal forests, podzolic soils prevail that comprise of a distinct upper organic humus/mor (O) horizon that is supported by underlying eluvial (E) and illuvial (B) mineral horizons. The dominant tree species, Scots pine (Pinus sylvestris L.), is known to be highly dependent on root symbiosis with ectomycorrhizal fungi that develop in constituent podzol horizons for growth in these nutrient limited soils. The aim of this microcosm-based study was a quantification of photosynthetically fixed 14C allocation, following standard pulse-feeding of 7-month-old Scots pine seedling shoots, to respective root and mycorrhizosphere compartments that developed in the reconstructed podzol (O, E and B) profile. Biomass of roots and mycorrhizas decreased with increasing soil depth but no soil origin, control forest vs. clear-cut area, related differences were observed. Similarly, no major soil origin- or podzol horizon-related differences in categorised ectomycorrhizal morphotypes and number of mycorrhizas, in relation to pooled root and mycorrhiza biomass, were detected. However, the total recovery of 14C-label was significantly higher in clear-cut soil microcosms compared to control counterparts. A significant finding was equivalent 14C-carbon allocation to roots and ectomycorrhizas in all three major, organic and mineral, podzol profile horizons studied. These carbon allocation data provide additional support for direct (or indirect) roles of roots and symbiotic mycorrhizal fungi in mineral weathering and biodegradation of organic ligands that are central for plant acquisition of growth limiting nutrients and the podzolization process in boreal forest ecosystems.

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References

  • Agerer R 2001 Exploration types of ectomycorrhizae: A proposal to classify ectomycorrhizal mycelial systems according to their patterns of differentiation and putative ecological importance. Mycorrhiza 11, 107–114.

    Google Scholar 

  • Baxter J W and Dighton J 2001 Ectomycorrhizal diversity alters growth and nutrient acquisition of grey birch (Betula populifolia) seedlings in host symbiotic culture conditions. New Phytol. 152, 139–149.

    Google Scholar 

  • Bending G D and Read D J 1995 The structure and function of the vegetative mycelium of ectomycorrhizal plants. V. Foraging behaviour and translocation of nutrients from exploited litter. New Phytol. 130, 401–409.

    Google Scholar 

  • Bidartondo M I, Ek H, Wallander H and Söderström B 2001 Do nutrient additions alter carbon sink strength of ectomycorrhizal fungi? New Phytol. 151, 543–550.

    Google Scholar 

  • Chen D M, Bastias B A, Taylor A F S and Cairney J W G 2003 Identification of laccase-like genes in ectomycorrhizal basidiomycetes and transcriptional regulation by nitrogen in Piloderma byssinum. New Phytol. 157, 547–554.

    Google Scholar 

  • Dahlberg A 2001 Community ecology of ectomycorrhizal fungi: an advancing interdisciplinary field. New Phytol. 150, 555–562.

    Google Scholar 

  • Dickie I A, Xu B and Koide R T 2002 Vertical niche differentiation of ectomycorrhizal hyphae in soil as shown by T-RFLP analysis. New Phytol. 156, 527–535.

    Google Scholar 

  • Dosskey M G, Linderman R G and Boersma L 1990 Carbon-sink stimulation of photosynthesis in Douglas fir seedlings by some ectomycorrhizas. New Phytol. 115, 269–274.

    Google Scholar 

  • Finlay R D and Read D J 1986 The structure and function of the vegetative mycelium of ectomycorrhizal plants. I. Translocation of 14C-labelled carbon between plants interconnected by a common mycelium. New Phytol. 103, 143–156.

    Google Scholar 

  • Finnish Statistical Yearbook of Forestry 1997 Ed. Y Sevola. Finnish Forest Research Institute, Gummerus Kirjapaino Oy, Jyväskylä.

    Google Scholar 

  • Fritze H, Pietikäinen J and Pennanen T 2000 Distribution of microbial biomass and phospholipid fatty acids in Podzol profiles under coniferous forest. Eur. J. of Soil Science 51, 565–573.

    Google Scholar 

  • Heinonsalo J, Jørgensen K and Sen R 2001 Microcosm-based analyses of Scots pine seedling growth, ectomycorrhizal fungal community structure and bacterial carbon utilization profiles in boreal forest humus and underlying illuvial mineral horizons. FEMS Microbiol. Ecol. 35, 73–84.

    Google Scholar 

  • Hemmilä I, Ståhlberg T and Mottram P (Eds.) 1994 Bioanalytical applications of labelling technologies. Wallac Oy, Turku, Finland.

    Google Scholar 

  • Högberg P, Nordgren A, Buchmann N, Taylor A F S, Ekblad A, Högberg M N, Nyberg G, Ottosson-Löfvenius M and Read D J 2001 Large-scale forest girdling shows that current photosynthesis drives soil respiration. Nature 411, 789–792.

    Google Scholar 

  • Ilvesniemi H, Giesler R, van Hees P, Magnusson T and Melkerud P A 2000 General description of the sampling techniques and the sites investigated in the Fennoscandinavian podzolization project. Geoderma 94, 109–123.

    Google Scholar 

  • Jansson K-J and Johansson J 1998 Soil changes after traffic with a tracked and a wheeled forest machine: a case study on a silt loam in Sweden. Forestry 71, 57–66.

    Google Scholar 

  • Jones M D, Durall D M and Cairney J W G 2003 Ectomycorrhizal fungal communities in young forest stands regenerating after clearcut logging. New Phytol. 157, 399–422

    Google Scholar 

  • Landeweert R, Hoffland E, Finlay R D, Kuyper T W and van Breemen N 2001 Linking plants to rocks: ectomycorrhizal fungi mobilize nutrients from minerals. Trends in Ecol. & Evol. 16, 248–254.

    Google Scholar 

  • Landeweert R, Leeflang P, Kuyper T W, Hoffland E, Rosling A, Wernars K and Smit E 2003 Molecular identification of ectomycorrhizal mycelium in soil horizons. Appl. Environ. Microbiol. 69, 327–333.

    Google Scholar 

  • Leake J R, Donnelly D P, Saunders E M, Boddy L and Read D J 2001 Rates and quantities of carbon flux to ectomycorrhizal mycelium following 14C pulse labeling of Pinus sylvestris seedlings: Effects of litter patches and interaction with a wood-decomposer fungus. Tree Physiol. 21, 71–82.

    Google Scholar 

  • Lundström U S, van Breemen N and Bain D 2000a The podzolization process. A review. Geoderma 94, 91–107.

    Google Scholar 

  • Lundström U S, van Breemen N, Bain D C, van Hees P A W, Giesler R, Gustafsson J P, Ilvesniemi H, Karltun E, Melkerud P-A, Olsson M, Riise G, Wahlberg O, Bergelin A, Bishop K, Finlay R, Jongmans A G, Magnusson T, Mannerkoski H, Nordgren A, Nyberg L, Starr M and Tau Strand L 2000b Advances in understanding the podzolization process resulting from a multidisciplinary study of three coniferous forest soils in the Nordic Countries. Geoderma 94, 335–353.

    Google Scholar 

  • Makkonen K and Helmisaari H-S 1998 Seasonal and yearly variations of fine-root biomass and necromass in a Scots pine (Pinus sylvestris L.) stand. For. Ecol.Manage. 102, 283–290.

    Google Scholar 

  • Mikola P, Hahl J and Torniainen E 1966 Vertical distribution of mycorrhizae in pine forests with spruce undergrowth. Ann. Bot. Fenn. 2, 406–409.

    Google Scholar 

  • Mogge B, Loferer C, Agerer R, Hutzler P and Hartmann A 2000 Bacterial community structure and colonization patterns of Fagus sylvatica L. ectomycorrhizospheres as determined by fluorescence in situ hybridization and confocal laser scanning microscopy. Mycorrhiza 9, 271–278.

    Google Scholar 

  • Perez-Moreno J and Read D J 2000 Mobilization and transfer of nutrients from litter to tree seedlings via the vegetative mycelium of ectomycorrhizal plants. New Phytol. 145, 301–309.

    Google Scholar 

  • Persson H Å 1983 The distribution and productivity of fine roots in boreal forests. Plant Soil 71, 87–101.

    Google Scholar 

  • Piirainen S, Finér L, Mannerkoski H and Starr M 2002 Effects of forest clear-cutting on the carbon and nitrogen fluxes through podzolic soil horizons. Plant Soil 239, 301–311.

    Google Scholar 

  • Read D J and Perez-Moreno J 2003 Mycorrhizas and nutrient cycling in ecosystems-A journey towards relevance? New Phytol. 157, 475–492.

    Google Scholar 

  • Rosling A, Landeweert R, Lindahl B D, Larsson K-H, Kuyper T W, Taylor A F S and Finlay R D 2003 Vertical distribution of ectomycorrhizal fungal taxa in a podzol soil profile. New Phytol. 159, 775–783.

    Google Scholar 

  • Rygiewicz P T and Andersen C P 1994 Mycorrhizae alter quality and quantity of carbon allocated below ground. Nature 369, 58–60.

    Google Scholar 

  • Smith S E and Read D J 1997 Mycorrhizal symbiosis, 2nd Edn., Academic Press, Cambridge.

    Google Scholar 

  • Sun Y-P, Unestam T, Lucas S D, Johanson K J, Kenne L and Finlay R 1999 Exudation-reabsorption in a mycorrhizal fungus, the dynamic interface for interaction with soil and soil microorganisms. Mycorrhiza 9, 137–144.

    Google Scholar 

  • Söderström B E 1979 Seasonal fluctuations of active fungal biomass in horizons of a podzolized pine-forest in central Sweden. Soil Biol. Biochem. 11, 149–154.

    Google Scholar 

  • Tamm C O 1991 Nitrogen in terrestrial ecosystems. Ecological Studies, Vol. 81. Berlin, Springer-Verlag.

    Google Scholar 

  • Tammi H, Timonen S and Sen R 2001 Spatiotemporal colonization of Scots pine roots by introduced and indigenous ectomycorrhizal fungi in forest humus and nursery Sphagnum peat microcosms. Can. J. For. Res. 31, 746–756.

    Google Scholar 

  • Timonen S, Tammi H and Sen R 1997 Characterization of the host genotype and fungal diversity in Scots pine ectomycorrhiza from natural humus microcosms using isozyme and PCR-RFLP analyses. New Phytol. 135, 313–323.

    Google Scholar 

  • Timonen S, Jorgensen K S, Haahtela K and Sen R 1998 Bacterial community structure at defined locations of Pinus sylvestris-Suillus bovinus mycorrhizospheres in dry pine forest humus and nursery peat. Can. J. Microbiol. 44, 499–513.

    Google Scholar 

  • Wallander H 2000 Uptake of P from apatite by Pinus sylvestris seedlings colonised by different ectomycorrhizal fungi. Plant Soil 218, 249–256.

    Google Scholar 

  • Wallander H and Wickman T 1999 Biotite and microcline as potassium sources in ectomycorrhizal and non-mycorrhizal Pinus sylvestris seedlings. Mycorrhiza 9, 25–32.

    Google Scholar 

  • van Breemen N, Finlay R D, Lundström U S, Jongmans A G, Giesler R and Olsson M 2000a Mycorrhizal weathering: a true case of plant mineral nutrition? Biogechemistry 49, 53–67.

    Google Scholar 

  • van Breemen N, Lundström U and Jongmans A G 2000b Do plants drive podzolisation via rock-eating mycorrhizal fungi? Geoderma 94, 163–171.

    Google Scholar 

  • Wu B, Nara K and Hogetsu T 2001 Can 14C-labeled photosynthetic products move between Pinus densiflora seedlings linked by ectomycorrhizal mycelia? New Phytol. 149, 137–146.

    Google Scholar 

  • Wu B, Nara T and Hogetsu T 2002 Spatiotemporal transfer of carbon-14-labelled photosynthate from ectomycorrhizal Pinus densiflora seedlings to extraradical mycelia. Mycorrhiza, 12, 83–88.

    Google Scholar 

  • Zvyagintsev D G 1994 Vertical disribution of microbial communities in soils. In Beyond the Biomass: Compositional and Functional Analysis of Soil Microbial Communities. Eds. K Ritz, J Dighton and K E Giller. pp. 29–38. Wiley, Chichester.

    Google Scholar 

  • Ågren G I, Axelsson B, Flower-Ellis J G K, Linder S, Persson H, Staaf H and Troeng E 1980 Annual carbon budget for a young Scots pine. In Structure and Function of Northern Coniferous Forests — An Ecosystem Study. Ed. T Persson. Ecol. Bull. (Stockholm) 32, 307–313.

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Heinonsalo, J., Hurme, KR. & Sen, R. Recent 14C-labelled assimilate allocation to Scots pine seedling root and mycorrhizosphere compartments developed on reconstructed podzol humus, E- and B- mineral horizons. Plant and Soil 259, 111–121 (2004). https://doi.org/10.1023/B:PLSO.0000020939.64205.c4

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  • DOI: https://doi.org/10.1023/B:PLSO.0000020939.64205.c4

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