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6 - Role of arbuscular mycorrhizal fungi in carbon and nutrient cycling in grassland

Published online by Cambridge University Press:  10 December 2009

By
David Johnson ,
Jonathan R. Leake  and
David J. Read
Edited by
Geoffrey Michael Gadd
David Johnson
Affiliation:
Department of Plant and Soil Science, University of Aberdeen, Cruickshank Building, St Machar Drive, Aberdeen AB24 3UU, UK
Jonathan R. Leake
Affiliation:
Department of Animal and Plant Science, University of Sheffield Alfred, Denny Building Western Bank Sheffield S10 2TN, UK
David J. Read
Affiliation:
Department of Animal and Plant Science, University of Sheffield Alfred, Denny Building Western Bank Sheffield S10 2TN, UK
Geoffrey Michael Gadd
Affiliation:
University of Dundee
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Summary

Introduction

Arbuscular mycorrhizal fungi (AMF) are the most ancient, widespread and ubiquitous of all the groups of mycorrhiza: they have a global distribution in widely contrasting plant communities including the Tropics, the Boreal forest, arctic tundra and all types of grassland. Considerable effort has been made in recent years in order to set AMF within a robust phylogeny. Recent advances in molecular biological techniques have enabled scientists to place AMF in a new division, the Glomeromycota. At present, this division contains only about 150 species, which is remarkable given the enormous number of plant species the fungi readily colonize. The mutualistic symbioses that AMF form with their host plants give rise to a number of important benefits to both the plant and fungus. A brief glance at a standard mycorrhizal text will list many ecologically important attributes, such as improved disease resistance, water uptake, nutrient transfer and the ability of the fungus to be a major sink for photosynthate. Indeed, the importance of AMF for nutrient uptake and carbon allocation has been recognized for decades. The ability of AMF (and other mycorrhizal types) to utilize recent plant photosynthate and thus have access to a near continuous supply of energy immediately gives them a potential advantage over saprotrophic micro-organisms, which are forced to obtain their energy in the highly carbon-limited heterogeneous soil environment.

Type
Chapter
Information
Fungi in Biogeochemical Cycles , pp. 129 - 150
Publisher: Cambridge University Press
Print publication year: 2006

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References

Ames, R. N., Mihara, K. L. & Baynes, H. G. (1989). Chitin-decomposing actinomycetes associated with a vesicular arbuscular mycorrhizal fungus from a calcareous grassland. New Phytologist, 111, 67–71.CrossRefGoogle Scholar
Anderson, J. P. E. & Domsch, K. H. (1978). A physiological method for the quantitative measurement of microbial biomass in soils. Soil Biology and Biochemistry, 10, 215–21.CrossRefGoogle Scholar
Bago, B., Zipfel, W., Williams, R. M.et al. (2002). Translocation and utilization of fungal storage lipid in the arbuscular mycorrhizal symbiosis. Plant Physiology, 128, 108–24.CrossRefGoogle ScholarPubMed
Bago, B., Pfeffer, P. E., Abubaker, J.et al. (2003). Carbon export from arbuscular mycorrhizal roots involves the translocation of carbohydrate as well as lipid. Plant Physiology, 131, 1496–507.CrossRefGoogle ScholarPubMed
Bardgett, R. D., Streeter, T. C. & Bol, R. (2003). Soil microbes compete effectively with plants for organic-nitrogen inputs to temperate grasslands. Ecology, 84, 1277–87.CrossRefGoogle Scholar
Boddington, C. L., Bassett, E. E., Jakobsen, I. & Dodd, J. C. (1999). Comparison of techniques for the extraction and quantification of extraradical mycelium of arbuscular mycorrhizal fungi in soils. Soil Biology and Biochemistry, 31, 479–82.CrossRefGoogle Scholar
Brookes, P. C., Powlson, D. S. & Jenkinson, D. S. (1982). Measurement of microbial biomass phosphorus in soil. Soil Biology and Biochemistry, 14, 319–29.CrossRefGoogle Scholar
Brookes, P. C., Landman, A., Pruden, G. & Jenkinson, D. S. (1985). Chloroform fumigation and the release of soil-nitrogen – a rapid direct extraction method to measure microbial biomass nitrogen in soil. Soil Biology and Biochemistry, 17, 837–42.CrossRefGoogle Scholar
Clark, R. B. & Zeto, S. K. (2000). Mineral acquisition by arbuscular mycorrhizal plants. Journal of Plant Nutrition, 23, 867–902.CrossRefGoogle Scholar
Fitter, A. H., Graves, J. D., Watkins, N. K., Robinson, D. & Scrimgeour, C. (1998). Carbon transfer between plants and its control in networks of arbuscular mycorrhizas. Functional Ecology, 12, 406–12.CrossRefGoogle Scholar
Francis, R. & Read, D. J. (1984). Direct transfer of carbon between plants connected by vesicular-arbuscular mycorrhizal mycelium. Nature, 307, 53–6.CrossRefGoogle Scholar
Frey, B., Vilarino, A., Schuepp, H. & Arines, J. (1994). Chitin and ergosterol content of extraradical and intraradical mycelium of the vesicular-arbuscular mycorrhizal fungus Glomus intraradices. Soil Biology and Biochemistry, 26, 711–17.CrossRefGoogle Scholar
Friese, C. F. & Allen, M. F. (1991). The spread of VA mycorrhizal fungal hyphae in soil: inoculum type and external hyphal architecture. Mycologia, 83, 409–18.CrossRefGoogle Scholar
Gallaud, I. (1905). Etudes sur les mycorrhizes endotrophs. Revue Générale de Botanique, 17, 5–48, 66–83, 123–35, 223–39, 313–25, 425–33, 479–500.Google Scholar
Grime, J. P., Mackey, J. M. L., Hillier, S. H. & Read, D. J. (1987). Floristic diversity in a model system using experimental microcosms. Nature, 328, 420–2.CrossRefGoogle Scholar
Hart, M. M. & Reader, R. J. (2002). Taxonomic basis for variation in the colonization strategy of arbuscular mycorrhizal fungi. New Phytologist, 153, 335–44.CrossRefGoogle Scholar
Hershey, A. D. & Chase, M. (1952). Independent functions of viral protein and nucleic acid in growth of bacteriophage. Journal of General Physiology, 36, 39–56.CrossRefGoogle ScholarPubMed
Ho, I. & Trappe, J. M. (1973). Translocation of 14C from Festuca plants to their endomycorrhizal fungi. Nature New Biology, 244, 30–1.CrossRefGoogle Scholar
Hodge, A., Campbell, C. D. & Fitter, A. H. (2001). An arbuscular mycorrhizal fungus accelerates decomposition and acquires nitrogen directly from organic material. Nature, 413, 297–9.CrossRefGoogle ScholarPubMed
Holtum, J. A. M. & Winter, K. (2003). Photosynthetic CO2 uptake in seedlings of two tropical tree species exposed to oscillating elevated concentrations of CO2. Planta, 218, 152–8.CrossRefGoogle ScholarPubMed
Jakobsen, I., Abbott, L. K. & Robson, A. D. (1992). External hyphae of vesicular-arbuscular mycorrhizal fungi associated with Trifolium subterraneum L. 1. Spread of hyphae and phosphorus inflow into roots. New Phytologist, 120, 371–80.CrossRefGoogle Scholar
Jenkinson, D. S. & Powlson, D. S. (1976). The effects of biocidal treatments on metabolism in soil V. A method for measuring soil biomass. Soil Biology and Biochemistry, 8, 209–13.CrossRefGoogle Scholar
Johnson, D., Leake, J. R. & Read, D. J. (2001). Novel in-growth core system enables functional studies of grassland mycorrhizal mycelial networks. New Phytologist, 152, 555–62.CrossRefGoogle Scholar
Johnson, D., Leake, J. R., Ostle, N., Ineson, P. & Read, D. J. (2002a). In situ 13CO2 pulse-labelling of upland grassland demonstrates a rapid pathway of carbon flux from arbuscular mycorrhizal mycelium to the soil. New Phytologist, 153, 327–34.CrossRefGoogle Scholar
Johnson, D., Leake, J. R. & Read, D. J. (2002b). Transfer of recent photosynthate into mycorrhizal mycelium of an upland grassland: short-term respiratory losses and accumulation of 14C. Soil Biology and Biochemistry, 34, 1521–4.CrossRefGoogle Scholar
Joner, E. J., Magid, J., Gahoonia, T. S. & Jakobsen, I. (1995). P depletion and activity of phosphatases in the rhizosphere of mycorrhizal and non-mycorrhizal cucumber (Cucumis sativus L). Soil Biology and Biochemistry, 27, 1145–51.CrossRefGoogle Scholar
Joner, E. J., Aarle, I. M. & Vosatka, M. (2000). Phosphatase activity of extraradical arbuscular mycorrhizal hyphae: a review. Plant and Soil, 226, 199–210.CrossRefGoogle Scholar
Jongmans, A. G., Breemen, N., Lundstrom, U.et al. (1997). Rock-eating fungi. Nature, 389, 682–3.CrossRefGoogle Scholar
Kabir, Z. & Koide, R. T. (2002). Effect of autumn and winter mycorrhizal cover crops on soil properties, nutrient uptake and yield of sweet corn in Pennsylvania, USA. Plant and Soil, 238, 205–15.CrossRefGoogle Scholar
Kabir, Z., O'Halloran, I. P., Widden, P. & Hamel, C. (1998). Vertical distribution of arbuscular mycorrhizal fungi under corn (Zea mays L.) in no-till and conventional tillage systems. Mycorrhiza, 8, 53–5.CrossRefGoogle Scholar
Knight, W. G., Allen, M. F., Jurinak, J. J. & Dudley, L. M. (1989). Elevated carbon-dioxide and solution phosphorus in soil with vesicular-arbuscular mycorrhizal western wheatgrass. Soil Science Society of America Journal, 53, 1075–82.CrossRefGoogle Scholar
Knight, W. G., Dudley, L. M. & Jurinak, J. J. (1992). Oxalate effects on solution phosphorus in a calcareous soil. Arid Soil Research Rehabilitation, 6, 11–20.CrossRefGoogle Scholar
Koide, R. T. & Kabir, Z. (2000). Extraradical hyphae of the mycorrhizal fungus Glomus intraradices can hydrolyse organic phosphate. New Phytologist, 148, 511–17.CrossRefGoogle Scholar
Kuzyakov, Y., Kretzschmar, A. & Stahr, K. (1999). Contribution of Lolium perenne rhizodeposition to carbon turnover of pasture soil. Plant and Soil, 213, 127–36.CrossRefGoogle Scholar
Kuzyakov, Y., Ehrensberger, H. & Stahr, K. (2001). Carbon partitioning and below-ground translocation by Lolium perenne. Soil Biology and Biochemistry, 33, 61–74.CrossRefGoogle Scholar
Langley, J. A. & Hungate, B. A. (2003). Mycorrhizal controls on below-ground litter quality. Ecology, 84, 2302–12.CrossRefGoogle Scholar
Leake, J. R., Donnelly, D. P., Saunders, E. M., Boddy, L. & Read, D. J. (2001). Rates and quantities of carbon flux to ectomycorrhizal mycelium following 14C pulse labelling of Pinus sylvestris seedlings: effects of litter patches and interaction with a wood-decomposer fungus. Tree Physiology, 21, 71–82.CrossRefGoogle Scholar
Leake, J. R., Johnson, D., Donnelly, D. P.et al. (2004). Networks of power and influence: the role of mycorrhizal mycelium in controlling plant communities and agroecosystem function. Canadian Journal of Botany, 82, 1016–45.CrossRefGoogle Scholar
Lerat, S., Lapointe, L., Piche, Y. & Vierheilig, H. (2003). Variable carbon-sink strength of different Glomus mosseae strains colonizing barley roots. Canadian Journal of Botany, 81, 886–9.CrossRefGoogle Scholar
Li, X. L., George, E. & Marschner, H. (1991). Phosphorus depletion and pH decrease at the root soil and hyphae soil interfaces of VA mycorrhizal white clover fertilized with ammonium. New Phytologist, 119, 397–404.CrossRefGoogle Scholar
Linkins, A. E. & Neal, J. L. (1982). Soil cellulase, chitinase, and protease activity in Eriophorum vaginatum tussock tundra in Eashle Summit, Alaska. Holarctic Ecology, 5, 135–8.Google Scholar
Lueders, T., Wagner, B., Claus, P. & Friedrich, M. W. (2004). Stable isotope probing of rRNA and DNA reveals a dynamic methylotroph community and trophic interactions with fungi and protozoa in oxic rice field soil. Environmental Microbiology, 6, 60–72.CrossRefGoogle ScholarPubMed
McGonigle, T. P. & Fitter, A. H. (1988). Ecological consequences of arthropod grazing on VA mycorrhizal fungi. Proceedings of the Royal Society of Edinburgh B, 94, 25–32.Google Scholar
McNaughton, S. J. & Oestenheld, M. (1990). Extramatrical mycorrhizal abundance and grass nutrition in a tropical grazing ecosystem, the Serengeti National Park, Tanzania. Oikos, 59, 92–6.CrossRefGoogle Scholar
Martin, J. K. & Merckx, R. (1992). The partitioning of photosynthetically fixed carbon within the rhizosphere of mature wheat. Soil Biology and Biochemistry, 24, 1147–56.CrossRefGoogle Scholar
Metcalfe, A. C., Krsek, M., Gooday, G. W., Prosser, J. I. & Wellington, E. M. H. (2002). Molecular analysis of a bacterial chitinolytic community in an upland pasture. Applied and Environmental Microbiology, 68, 5042–50.CrossRefGoogle Scholar
Miller, R. M., Reinhardt, D. R. & Jastrow, J. D. (1995). External hyphal production of vesicular-arbuscular mycorrhizal fungi in pasture and tallgrass prairie communities. Oecologia, 103, 17–23.CrossRefGoogle ScholarPubMed
Munkvold, L., Kjøller, R., Vestberg, M., Rosendahl, S. & Jakobsen, I. (2004). High functional diversity within species of arbuscular mycorrhizal fungi. New Phytologist, 164, 357–64.CrossRefGoogle Scholar
Nehl, D. B., McGee, P. A., Torrisi, V., Pattinson, G. S. & Allen, S. J. (1999). Patterns of arbuscular mycorrhiza down the profile of a heavy textured soil do not reflect associated colonization potential. New Phytologist, 142, 495–503.CrossRefGoogle Scholar
Olsrud, M. & Christensen, T. R. (2004). Carbon cycling in subarctic tundra; seasonal variation in ecosystem partitioning based on in situ14C pulse-labelling. Soil Biology and Biochemistry, 36, 245–53.CrossRefGoogle Scholar
Olsson, P. A. & Wilhelmsson, P. (2000). The growth of external AM fungal mycelium in sand dunes and in experimental systems. Plant and Soil, 226, 161–9.CrossRefGoogle Scholar
Olsson, P. A., Bååth, E., Jakobsen, I. & Söderström, B. (1995). The use of phospholipid and neutral lipid fatty acids to estimate biomass of arbuscular mycorrhizal fungi in soil. Mycological Research, 99, 623–9.CrossRefGoogle Scholar
Olsson, P. A., Larsson, L., Bago, B., Wallander, H. & Aarle, I. M. (2003). Ergosterol and fatty acids for biomass estimation of mycorrhizal fungi. New Phytologist, 159, 7–10.CrossRefGoogle Scholar
Ostle, N., Ineson, P., Benham, D. & Sleep, D. (2000). Carbon assimilation and turnover in grassland vegetation using an in situ13CO2 pulse labelling system. Rapid Communications Mass Spectrometry, 14, 1345–50.3.0.CO;2-B>CrossRefGoogle Scholar
Paul, E. A. & Kucey, R. M. N. (1981). Carbon flow in plant microbial associations. Science, 213, 473–4.CrossRefGoogle ScholarPubMed
Pfeffer, P. E., Douds, D. D., Becard, G. & Shachar-Hill, Y. (1999). Carbon uptake and the metabolism and transport of lipids in an arbuscular mycorrhiza. Plant Physiology, 120, 587–98.CrossRefGoogle Scholar
Powell, C. L. (1979). Spread of mycorrhizal fungi through soil. New Zealand Journal of Agricultural Research, 22, 335–9.CrossRefGoogle Scholar
Radajewski, S., Ineson, P., Parekh, N. R. & Murrell, J. C. (2000). Stable-isotope probing as a tool in microbial ecology. Nature, 403, 646–9.CrossRefGoogle ScholarPubMed
Read, D. J.(2002). Towards ecological relevance – progress and pitfalls in the path towards an understanding of mycorrhizal functions in nature. In Mycorrhizal Ecology, ed. Heijden, M. G. A. & Sanders, I. R.. Berlin: Springer-verlag, pp. 3–24.Google Scholar
Read, D. J., Koucheki, H. K. & Hodgson, J. (1976). Vesicular-arbuscular mycorrhiza in natural vegetation systems. I. The occurrence of infection. New Phytologist, 77, 641–53.CrossRefGoogle Scholar
Rillig, M. C., Wright, S. F. & Eviner, V. T. (2002). The role of arbuscular mycorrhizal fungi and glomalin in soil aggregation: comparing effects of five plant species. Plant and Soil, 238, 325–33.CrossRefGoogle Scholar
Saggar, S., Hedley, C. & Mackay, A. D. (1997). Partitioning and translocation of photosynthetically fixed 14C in grazed hill pastures. Biology and Fertility of Soils, 25, 152–8.CrossRefGoogle Scholar
Sparling, G. P. & Tinker, P. B. (1978). Mycorrhizal infection in Pennine grassland. I. Levels of infection in the field. Journal of Applied Ecology, 15, 943–950.CrossRefGoogle Scholar
Staddon, P. L., Ostle, N., Dawson, L. A. & Fitter, A. H. (2003a). The speed of soil carbon throughput in an upland grassland is increased by liming. Journal of Experimental Botany, 54, 1461–1469.CrossRefGoogle Scholar
Staddon, P. L., Ramsey, C. B., Ostle, N., Ineson, P. & Fitter, A. H. (2003b). Rapid turnover of hyphae of mycorrhizal fungi determined by AMS microanalysis of 14C. Science, 300, 1138–1140.CrossRefGoogle Scholar
Staddon, P. L., Thompson, K., Jakobsen, I.et al. (2003c). Mycorrhizal fungal abundance is affected by long-term climatic manipulations in the field. Global Change Biology, 9, 186–94.CrossRefGoogle Scholar
Sylvia, D. M. (1988). Activity of external hyphae of vesicular-arbuscular mycorrhizal fungi. Soil Biology and Biochemistry, 20, 39–43.CrossRefGoogle Scholar
Tarafdar, J. C. & Marschner, H. (1994). Phosphatase-activity in the rhizosphere and hyphosphere of VA mycorrhizal wheat supplied with inorganic and organic phosphorus. Soil Biology and Biochemistry, 26, 387–95.CrossRefGoogle Scholar
Tisdall, J. M. & Oades, J. M. (1979). Stabilization of soil aggregates by the root systems of ryegrass. Australian Journal of Soil Research, 17, 429–41.CrossRefGoogle Scholar
Toal, M. E., Yeomans, C., Killham, K. & Meharg, A. A. (2000). A review of rhizosphere carbon flow modelling. Plant and Soil, 222, 263–81.CrossRefGoogle Scholar
Treseder, K. K. & Allen, M. F. (2000). Mycorrhizal fungi have a potential role in soil carbon storage under elevated CO2 and nitrogen deposition. New Phytologist, 147, 189–200.CrossRefGoogle Scholar
Treseder, K. K., Egerton-Warburton, L. M., Allen, M. F., Cheng, Y. F. & Oechel, W. C. (2003). Alteration of soil carbon pools and communities of mycorrhizal fungi in chaparral exposed to elevated carbon dioxide. Ecosystems, 6, 786–96.CrossRefGoogle Scholar
Heijden, M. G. A., Klironomos, J. N., Ursic, M.et al. (1998). Mycorrhizal fungal diversity determines plant biodiversity, ecosystem variability and productivity. Nature, 396, 69–72.CrossRefGoogle Scholar
Hees, P. A. W., Godbold, D. L., Jentschke, G. & Jones, D. L. (2003). Impact of ectomycorrhizas on the concentration and biodegradation of simple organic acids in a forest soil. European Journal of Soil Science, 54, 697–706.CrossRefGoogle Scholar
Vandenkoornhuyse, P., Leyval, C. & Bonnin, I. (2001). High genetic diversity in arbuscular mycorrhizal fungi: evidence for recombination events. Heredity, 87, 243–53.CrossRefGoogle ScholarPubMed
Vandenkoornhuyse, P., Baldauf, S. L., Leyval, C., Straczek, J. & Young, J. P. W. (2002). Extensive fungal diversity in plant roots. Science, 295, 2051.CrossRefGoogle ScholarPubMed
Wagner, G. (1974). Observation of fungal growth in soil using a capillary pedoscope. Soil Biology and Biochemistry, 6, 327–33.CrossRefGoogle Scholar
Warnock, A. J., Fitter, A. H. & Usher, M. B. (1982). The influence of a springtail Folsomia candida (Insecta, Collembola) on the mycorrhizal association of leek Allium porrum and the vesicular-mycorrhizal endophyte Glomus fasciculatus. New Phytologist, 90, 285–92.CrossRefGoogle Scholar
Weigelt, A., King, R., Bol, R. & Bardgett, R. D. (2003). Inter-specific variability in organic nitrogen uptake of three temperate grassland species. Journal of Plant Nutrition and Soil Science, 166, 606–11.CrossRefGoogle Scholar
Zhu, Y. G. & Miller, R. M. (2003). Carbon cycling by arbuscular mycorrhizal fungi in soil-plant systems. Trends in Plant Science, 8, 407–9.CrossRefGoogle ScholarPubMed

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