Skip to main content Accessibility help
×
Hostname: page-component-cd9895bd7-dzt6s Total loading time: 0 Render date: 2024-12-24T14:45:00.906Z Has data issue: false hasContentIssue false

3 - Fungal roles in transport processes in soils

Published online by Cambridge University Press:  10 December 2009

Karl Ritz
Affiliation:
National Soil Resources Institute, Cranfield University, UK
Geoffrey Michael Gadd
Affiliation:
University of Dundee
Get access

Summary

Introduction

Fundamentally, biogeochemical cycling involves the transformation of compounds between various forms, and a movement of such compounds within and between compartments of the biosphere and geosphere. These processes operate across a wide range of spatial and temporal scales, from micrometres to kilometres, from seconds to centuries. In terrestrial systems, transformations and movement of materials below-ground are governed by the spatial organization of the soil system, and particularly the architecture of the pore network. This ‘inner space’ provides the physical framework in and through which the majority of soil-based processes occur. The labyrinthine nature of the pore network, and the exchange properties of associated surfaces, strongly modulates the transport of materials through the soil matrix. From a physicochemical perspective soil structure generally retards transport processes for two main reasons: the complex geometry of the pore network increases path lengths, both for diffusive and bulk-flow movement; and charged mineral and organic constituents in the soil act as exchange surfaces which bind transportable compounds to varying degrees. Transport processes may also be accelerated by structural properties, for example if solutes or particulates are carried via preferential and bypass-flow channels of water through macropores.

Soil organisms play a key role in driving terrestrial nutrient cycling, and play both direct and indirect roles in effecting and affecting transport processes. Fungi contribute a particularly wide range of functions relating to nutrient cycling.

Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2006

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Amir, R., Steudle, E., Levanon, D., Hadar, Y. & Chet, I. (1995). Turgor changes in Morchella esculenta during translocation and sclerotial formation. Experimental Mycology, 19, 129–36.CrossRefGoogle Scholar
Anderson, P., Davidson, C. M., Littlejohn, D.et al. (1997). The translocation of caesium and silver by fungi in some Scottish soils. Communications in Soil Science and Plant Analysis, 28, 635–50.CrossRefGoogle Scholar
Arnebrant, K., Ek, H., Finlay, R. D. & Söderström, B. (1993). Nitrogen translocation between Alnus glutinosa (L.) Gaertn. seedlings inoculated with Frankia sp. and Pinus contorta Doug. ex Loud seedlings connected by a common ectomycorrhizal mycelium. New Phytologist, 124, 213–42.CrossRefGoogle Scholar
Bago, B., Pfeffer, P. E., Zipfel, W., Lammers, P. & Shachar-Hill, Y. (2002). Tracking metabolism and imaging transport in arbuscular mycorrhizal fungi. Metabolism and transport in AM fungi. Plant and Soil, 244, 189–97.CrossRefGoogle Scholar
Bakken, L. R. & Olsen, R. A. (1990). Accumulation of radiocaesium in fungi. Canadian Journal of Microbiology, 36, 704–10.CrossRefGoogle ScholarPubMed
Bethlenfalvay, G. J., Reyes-Solis, M. G., Camel, S. B. & Ferrera-Cerrato, R. (1991). Nutrient transfer between the root zones of soybean and maize plants connected by a common mycorrhizal mycelium. Physiologia Plantarum, 82, 423–32.CrossRefGoogle Scholar
Boddy, L. (1999). Saprotrophic cord-forming fungi: meeting the challenge of heterogeneous environments. Mycologia, 91, 13–32.CrossRefGoogle Scholar
Bolton, R. G. & Boddy, L. (1993). Characterisation of the spatial aspects of foraging mycelial cord systems using fractal geometry. Mycological Research, 97, 762–8.CrossRefGoogle Scholar
Boswell, G. P., Jacobs, H., Davidson, F. A., Gadd, G. M. & Ritz, K. (2002). Functional consequences of nutrient translocation in mycelial fungi. Journal of Theoretical Biology, 217, 459–77.CrossRefGoogle ScholarPubMed
Boswell, G. P., Jacobs, H., Davidson, F. A., Gadd, G. M. & Ritz, K. (2003). Growth and function of fungal mycelia in heterogeneous environments. Bulletin of Mathematical Biology, 65, 447–77.CrossRefGoogle ScholarPubMed
Brownlee, C. & Jennings, D. H. (1982). Long-distance translocation in Serpula lacrymans: velocity estimates and the continuous monitoring of induced perturbations. Transactions of the British Mycological Society, 79, 143–8.CrossRefGoogle Scholar
Cairney, J. W. G. (1992). Translocation of solutes in ectomycorrhizal and saprotrophic rhizomorphs. Mycological Research, 96, 135–41.CrossRefGoogle Scholar
Cairney, J. W. G. & Burke, R. M. (1996). Physiological heterogeneity within fungal mycelia: an important concept for a functional understanding of the ectomycorrhizal symbiosis. New Phytologist, 134, 685–95.CrossRefGoogle Scholar
Caris, C., Hordt, W., Hawkins, H. J., Romheld, V. & George, E. (1998). Studies of iron transport by arbuscular mycorrhizal hyphae from soil to peanut and sorghum plants. Mycorrhiza, 8, 35–9.CrossRefGoogle Scholar
Cole, L., Orlovich, D. A. & Ashford, A. E. (1998). Structure, function and motility of vacuoles in filamentous fungi. Fungal Genetics and Biology, 24, 86–100.CrossRefGoogle ScholarPubMed
Davidson, F. A. & Olsson, S. (2000). Translocation induced outgrowth of fungi in nutrient-free environments. Journal of Theoretical Biology, 205, 73–84.CrossRefGoogle ScholarPubMed
Declerck, S., Dupre de Boulois, H., Bivort, C. & Delvaux, B. (2003). Extraradical mycelium of the arbuscular mycorrhizal fungus Glomus lamellosum can take up, accumulate and translocate radiocaesium under root-organ culture conditions. Environmental Microbiology, 5, 510–16.CrossRefGoogle ScholarPubMed
Finlay, R. & Read, D. J. (1986a). The structure and function of the vegetative mycelium of ectomycorrhizal plants.1. Translocation of 14C-labelled carbon between plants interconnected by a common mycelium. New Phytologist, 103, 143–56.CrossRefGoogle Scholar
Finlay, R. & Read, D. J.(1986b). The structure and function of the vegetative mycelium of ectomycorrhizal plants. 2. The uptake and distribution of phosphorus by mycelium interconnecting host plants. New Phytologist, 103, 157–65.CrossRefGoogle Scholar
Frey, S. D., Elliott, E. T., Paustian, K. & Peterson, G. A. (2000). Fungal translocation as a mechanism for soil nitrogen inputs to surface residue decomposition in a no-tillage agroecosystem. Soil Biology and Biochemistry, 32, 689–98.CrossRefGoogle Scholar
Frey, S. D., Six, J. & Elliott, E. T. (2003). Reciprocal transfer of carbon and nitrogen by decomposer fungi at the soil-litter interface. Soil Biology and Biochemistry, 35, 1001–4.CrossRefGoogle Scholar
George, E., Haussler, K. U., Vetterlein, D., Gorgus, E. & Marschner, H. (1992). Water and nutrient translocation by hyphae of Glomus mosseae. Canadian Journal of Botany, 70, 2130–7.CrossRefGoogle Scholar
Graves, J. D., Watkins, N. K., Fitter, A. H., Robinson, D. & Scrimgeour, C. (1997). Intraspecific transfer of carbon between plants linked by a common mycorrhizal network. Plant and Soil, 192, 153–9.CrossRefGoogle Scholar
Gray, S. N., Dighton, J., Olsson, S. & Jennings, D. H. (1995). Real-time measurement of uptake and translocation of 137Cs within mycelium of Schizophyllum commune Fr by autoradiography followed by quantitative image-analysis. New Phytologist, 129, 449–65.CrossRefGoogle Scholar
Harley, J. L. & Smith, S. E. (1983). Mycorrhizal Symbiosis. London: Academic Press.Google Scholar
Harris, K., Young, I. M., Gilligan, C. A., Otten, W. & Ritz, K. (2003). Effect of bulk density on the spatial organization of the fungus Rhizoctonia solani in soil. FEMS Microbiology Ecology, 44, 45–56.CrossRefGoogle ScholarPubMed
Hart, S. C., Firestone, M. K., Paul, E. A. & Smith, J. L. (1993). Flow and fate of soil nitrogen in an annual grassland and a young mixed-conifer forest. Soil Biology and Biochemistry, 25, 431–42.CrossRefGoogle Scholar
Haselwandter, K., Berrek, M. & Brunner, P. (1988). Fungi as bioindicators of radiocaesium contamination: pre- and post-Chernobyl activities. Transactions of the British Mycological Society, 90, 171–4.CrossRefGoogle Scholar
Heap, A. J. & Newman, E. I. (1980). Links between roots by hyphae of vesicular-arbuscular mycorrhizas. New Phytologist, 85, 169–71.CrossRefGoogle Scholar
Hirrel, M. C. & Gerdemann, J. W. (1979). Enhanced carbon transfer between onions infected with a vesicular-arbuscular mycorrhizal fungus. New Phytologist, 83, 731–8.CrossRefGoogle Scholar
Howard, A. J. (1978). Translocation in fungi. Transactions of the British Mycological Society, 70, 265–9.CrossRefGoogle Scholar
Jacobs, H., Boswell, G. P., Scrimgeour, C. M.et al. (2004). Translocation of carbon by Rhizoctonia solani in nutritionally-heterogeneous microcosms. Mycological Research, 108, 453–62.CrossRefGoogle ScholarPubMed
Jansa, J., Mozafar, A. & Frossard, E. (2003). Long-distance transport of P and Zn through the hyphae of an arbuscular mycorrhizal fungus in symbiosis with maize. Agronomie, 23, 481–8.CrossRefGoogle Scholar
Jennings, D. H. (1987). Translocation of solutes in fungi. Biological Reviews, 62, 215–243.CrossRefGoogle Scholar
Jennings, D. H., Thornton, J. D., Galpin, M. F. J. & Coggins, C. R. (1974). Translocation in fungi. In Transport at the Cellular Level, ed. Sleigh, M. A. & Jennings, D. H.. Cambridge: Cambridge University Press, pp. 139–56.Google Scholar
Johansen, A. & Jensen, E. S. (1996). Transfer of N and P from intact or decomposing roots of pea to barley interconnected by an arbuscular mycorrhizal fungus. Soil Biology and Biochemistry, 28, 73–81.CrossRefGoogle Scholar
Johansen, A., Jakobsen, I. & Jensen, E. S. (1993). Hyphal transport by a vesicular-arbuscular mycorrhizal fungus of N applied to the soil as ammonium or nitrate. Biology and Fertility of Soils, 16, 66–70.CrossRefGoogle Scholar
Kirchner, G. & Daillant, O. (1998). Accumulation of 210Pb, 226Ra and radioactive cesium by fungi. Science of the Total Environment, 222, 63–70.CrossRefGoogle ScholarPubMed
Lindahl, B. D. & Olsson, S. (2004). Fungal translocation – creating and responding to environmental heterogeneity. Mycologist, 18, 79–88.CrossRefGoogle Scholar
Lindahl, B., Stenlid, J., Olsson, S. & Finlay, R. (1999). Translocation of 32P between interacting mycelia of a wood-decomposing fungus and ectomycorrhizal fungi in microcosm systems. New Phytologist, 144, 183–93.CrossRefGoogle Scholar
Lindahl, B., Finlay, R. & Olsson, S. (2001). Simultaneous, bidirectional translocation of 32P and 33P between wood blocks connected by mycelial cords of Hypholoma fasciculare. New Phytologist, 150, 189–94.CrossRefGoogle Scholar
Littlefield, L. J. (1967). Phosphorus-32 accumulation in Rhizoctonia solani sclerotia. Phytopathology, 57, 1053–5.Google Scholar
Mihail, J. D., Obert, M., Bruhn, J. N. & Taylor, S. J. (1995). Fractal geometry of diffuse mycelia and rhizomorphs of Armillaria species. Mycological Research, 99, 81–8.CrossRefGoogle Scholar
Money, N. P. (2004). The fungal dining habit – a biomechanical perspective. Mycologist, 18, 71–6.CrossRefGoogle Scholar
Newman, E. I. (1988). Mycorrhizal links between plants: their functioning and ecological significance. Advances in Ecological Research, 18, 243–70.CrossRefGoogle Scholar
Newman, E. I. & Eason, W. R. (1993). Rates of phosphorus transfer within and between ryegrass (Lolium perenne) plants. Functional Ecology, 7, 242–8.CrossRefGoogle Scholar
Niksic, M., Hadzic, I. & Glisic, M. (2004). Is Phallus impudicus a mycological giant?Mycologist, 18, 21–2.CrossRefGoogle Scholar
Olsson, S. (1995). Mycelial density profiles of fungi on heterogeneous media and their interpretation in terms of nutrient reallocation patterns. Mycological Research, 99, 143–53.CrossRefGoogle Scholar
Olsson, S. & Gray, S. N. (1998). Patterns and dynamics of 32P-phosphate and labelled 2-aminoisobutyric acid (C14-AIB) translocation in intact basidiomycete mycelia. FEMS Microbiology Ecology, 26, 109–20.CrossRefGoogle Scholar
Olsson, S. & Hansson, B. S. (1995). Action potential-like activity found in fungal mycelia is sensitive to stimulation. Naturwissenschaften, 82, 30–1.CrossRefGoogle Scholar
Olsson, S. & Persson, Y. (1994). Transfer of phosphorus from Rhizoctonia solani to the mycoparasite Arthrobotrys oligospora. Mycological Research, 98, 1065–8.CrossRefGoogle Scholar
Otten, W., Gilligan, C. A., Watts, C. W., Dexter, A. R. & Hall, D. (1999). Continuity of air-filled pores and invasion thresholds for a soil-borne fungal plant pathogen, Rhizoctonia solani. Soil Biology and Biochemistry, 31, 1803–10.CrossRefGoogle Scholar
Pfeffer, P. E., Douds, D. D., Bucking, H., Schwartz, D. P. & Shachar-Hill, Y. (2004). The fungus does not transfer carbon to or between roots in an arbuscular mycorrhizal symbiosis. New Phytologist, 163, 617–27.CrossRefGoogle Scholar
Rafferty, B., Brennan, M. & Kliashtorin, A. (1997). Decomposition in two pine forests: the mobilisation of 137Cs and K from forest litter. Soil Biology and Biochemistry, 29, 1673–81.CrossRefGoogle Scholar
Rayner, A. D. M. (1991). The challenge of the individualistic mycelium. Mycologia, 83, 48–71.CrossRefGoogle Scholar
Rayner, A. D. M. (1994). Pattern-generating processes in fungal communities. In Beyond the Biomass: Compositional and Functional Analysis of Soil Microbial Communities, ed. Ritz, K., Dighton, J. & Giller, K. E.. Chichester, UK: John Wiley, pp. 247–58.Google Scholar
Rayner, A. D. M. & Boddy, L. (1988). Fungal communities in the decay of wood. Advances in Microbial Ecology, 10, 155–63.Google Scholar
Read, D. J. & Stribley, D. P. (1975). Diffusion and translocation in some fungal culture systems. Transactions of the British Mycological Society, 64, 381–8.CrossRefGoogle Scholar
Ritz, K. (1995). Growth responses of some soil fungi to spatially heterogeneous nutrients. FEMS Microbiology Ecology, 16, 269–80.CrossRefGoogle Scholar
Ritz, K. & Crawford, J. W. (1990). Quantification of the fractal nature of colonies of Trichoderma viride. Mycological Research, 94, 1138–42.CrossRefGoogle Scholar
Ritz, K. & Newman, E. I. (1984). Movement of 32P between intact grassland plants of the same age. Oikos, 43, 138–42.CrossRefGoogle Scholar
Ritz, K. & Newman, E. I. (1986). Nutrient transport between ryegrass plants differing in nutrient status. Oecologia, 70, 128–31.CrossRefGoogle Scholar
Ritz, K. & Young, I. M. (2004). Interactions between soil structure and fungi. Mycologist, 18, 52–9.CrossRefGoogle Scholar
Ritz, K., Millar, S. M. & Crawford, J. W. (1996). Detailed visualisation of hyphal distribution in fungal mycelia growing in heterogeneous nutritional environments. Journal of Microbiological Methods, 25, 23–8.CrossRefGoogle Scholar
Rufyikiri, G., Thiry, Y. & Declerck, S. (2003). Contribution of hyphae and roots to uranium uptake and translocation by arbuscular mycorrhizal carrot roots under root-organ culture conditions. New Phytologist, 158, 391–9.CrossRefGoogle Scholar
Schütte, K. H. (1956). Translocation in the fungi. New Phytologist, 55, 164–82.CrossRefGoogle Scholar
Shepherd, V. A., Orlovich, D. A. & Ashford, A. E. (1993). A dynamic continuum of pleiomorphic tubules and vacuoles in growing hyphae of a fungus. Journal of Cell Science, 104, 495–507.Google Scholar
Simard, S., Perry, D. A., Jones, M. D.et al. (1997). Net transfer of carbon between ectomycorrhizal tree species in the field. Nature, 388, 579–82.CrossRefGoogle Scholar
Smith, S. E. & Read, D. J. (1997). Mycorrhizal Symbiosis. London: Academic Press.Google Scholar
Stahl, P. D. & Christensen, M. (1992). In vitro mycelial interactions among members of a soil micro-fungal community. Soil Biology and Biochemistry, 24, 309–16.CrossRefGoogle Scholar
Steinberg, G. (1998). Organelle transport and molecular motors in fungi. Fungal Genetics and Biology, 24, 161–77.CrossRefGoogle ScholarPubMed
Suzuki, H., Kumagai, H., Oohashi, K.et al. (2001). Transport of trace elements through the hyphae of an arbuscular mycorrhizal fungus into marigold determined by the multitracer technique. Soil Science and Plant Nutrition, 47, 131–7.CrossRefGoogle Scholar
Thrower, L. B. & Thrower, S. L. (1968). Movement of nutrients in fungi. II. The effect of reproductive structures. Australian Journal of Botany, 16, 81–7.CrossRefGoogle Scholar
Tlalka, M., Watkinson, S. C., Darrah, P. R. & Fricker, M. D. (2002). Continuous imaging of amino acid translocation in intact mycelia of Phanerochaete velutina reveals rapid, pulsatile fluxes. New Phytologist, 153, 173–84.CrossRefGoogle Scholar
Watkins, N. K., Fitter, A. H., Graves, J. D. & Robinson, D. (1996). Quantification using stable carbon isotopes of carbon transfer between C3 and C4 plants linked by a common mycorrhizal network. Soil Biology and Biochemistry, 28, 471–7.CrossRefGoogle Scholar
Wells, J. M. & Boddy, L. (1995a). Phosphorus translocation by saprotrophic basidiomycete mycelial cord systems on the floor of a mixed deciduous woodland. Mycological Research, 99, 977–80.CrossRefGoogle Scholar
Wells, J. M. & Boddy, L. (1995b). Translocation of soil-derived phosphorus in mycelial cord systems in relation to inoculum resource size. FEMS Microbiology Ecology, 17, 67–75.CrossRefGoogle Scholar
Wells, J. M., Boddy, L. & Evans, R. (1995). Carbon translocation in mycelial cord systems of Phanerochaete velutina (DC.: Pers.) Parmasto. New Phytologist, 129, 467–76.CrossRefGoogle Scholar
Wilcoxson, R. D. & Sudia, T. W. (1968). Translocation in fungi. Botanical Reviews, 34, 32–50.CrossRefGoogle Scholar

Save book to Kindle

To save this book to your Kindle, first ensure [email protected] is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×