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Thoughts on the processes that maintain local species diversity of ectomycorrhizal fungi

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The Significance and Regulation of Soil Biodiversity

Part of the book series: Developments in Plant and Soil Sciences ((DPSS,volume 63))

Abstract

Ectomycorrhizal fungi exhibit high diversity even in small monoculture forests. Roughly 20 to 35 species typically occupy such sites. Explanations for this diversity can be based on resource partitioning, disturbance, competition, or interaction with other organisms. Mycorrhizal fungi compete for two general classes of resources: host-derived carbon and soil or detritus derived mineral nutrients. Both types of resources are arrayed in space (e.g., soil depth, distance from tree) and time (e.g., season, host successional series). Some species seem to be partitioned in space and time at these scales, but the question of how widespread these patterns are remains largely unanswered. Mineral resources are distributed in discrete substrates in soil, litter, and within other soil microorganisms; the biochemical diversity exhibited by fungi may translate into differences in access to these resources among species. Small-scale natural disturbances that sever roots, mix soil horizons and litter layers, or change local pH and nutrient availability, are likely to create additional habitats for ectomycorrhizal fungi. Evidence from fruiting patterns and differences in colonization strategies suggest that such disturbances may be important for establishment of some species. Competitive replacement networks among species have the theoretical potential to increase diversity. The frequency of species replacements, observed co-infections of ectomycorrhizal fungi on single host roots, and high rates of rootlet turn-over all suggest that competition is important, but whether it plays a creative role in maintaining diversity remains to be demonstrated. Other organisms could be important in the maintenance of diversity, if they effect competition among mycorrhizal fungi. Bacteria and soil invertebrates are the most likely groups for such interactions. Technological advances in root observation and PCR methods for identification of mycorrhizae make many of these theories testable.

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References

  • Abuzinadah R A and Read D J 1986 The role of proteins in the nitrogen nutrition of ectomycorrhizal plants. I. Utilization of peptides and proteins by ectomycorrhizal fungi. New Phytol. 103, 481–493.

    Article  CAS  Google Scholar 

  • Agerer R 1990 Studies on ectomycorrhizae. 24. Ectomycorrhizae of Chroogomphus helveticus and C. rutilus (Gomphidiaceae, Basid-iomyetes) and their relationship to those of Suillus and Rhizo-pogon. Nova Hedwigia 50, 1–63.

    Google Scholar 

  • Armstrong R A 1976 Fugitive species: experiments with fungi and some theoretical considerations. Ecology 57, 53–963.

    Google Scholar 

  • Antibus R K, Croxdale J G, Miller O K and Linkins A E 1981 Ectomycorrhizal fungi of Salix rotundifolia III. Resynthesized mycorrhizal complexes and their surface phosphatase activities. Can. J. Bot. 59, 2458–2456.

    Article  Google Scholar 

  • Barron G L 1988 Microcolonies of bacteria as a nutrient source for lignicolous and other fungi. Can. J. Bot. 66, 2505–2510.

    Article  Google Scholar 

  • Bell E A and Janzen D H 1971 Medical and ecological consideration of L-dopa and 5-HTP in seeds. Nature 299, 136–137.

    Article  Google Scholar 

  • Berbee M L and Taylor J W 1993 Dating of the evolutionary radiations of the true fungi. Can. J. Bot. 71, 1114–1127.

    Article  Google Scholar 

  • Bills G F, Holtzmann G I and Miller O K Jr 1986 Comparison of ectomycorrhizal-basidiomycete communities in red spruce versus northern hardwood forests of West Virginia. Can. J. Bot. 64, 760–768.

    Article  Google Scholar 

  • Bowen G D and Theodorou C 1979 Interactions between bacteria and ectomycorrhizal fungi. Soil Biol. Biochem. 11, 119–126.

    Article  Google Scholar 

  • Bruns T D 1982 Insect mycophagy in the Boletales: fungivore diversity and the mushroom habitat. In Fungus Insect Relationships: Perspectives in Ecology and Evolution. Eds. Q Wheeler and M Blackwell. pp 91–129. Columbia Univ. Press, New York.

    Google Scholar 

  • Bruns T D and Gardes M 1993 Molecular tools for the identification of ectomycorrhizal fungi: taxon-specific oligonucleotide probes for suilloid fungi. Mol. Ecol. 2, 233–242.

    Article  PubMed  CAS  Google Scholar 

  • Buss L W and Jackson J B C 1979 Competitive networks: nontransitive competitive relationships in cryptic coral reef environments. Am. Nat. 113, 223–23.

    Article  Google Scholar 

  • Caldwell B A 1991 Fatty acid esterase production by ectomycor-rhizal fungi. Mycologia 83, 233–236.

    Article  CAS  Google Scholar 

  • Castellano M A and Molina R 1989 The biological component: nursery pests and mycorrhizae. In The Container Tree Nursery Manual. Vol. 5. Eds. T D Landis, R W Tinus, S E McDonald and J P Barnett. pp 101–167. USDA Forest Service, Washington, DC.

    Google Scholar 

  • Cibula W G and Ovrebo C L 1988 Mycosociological studies of mycorrhizal fungi in two loblolly pine plots in Mississippi and some relationships with remote sensing. In Remote Sensing for Resource Inventory, Planning and Monitoring. Proceedings of the 2nd Forest Service Remote Sensing Application conference, Ed. J D Greer. pp 268–307. Am. Soc. Photogram. Rem. Sens., Falls Church, VA

    Google Scholar 

  • Colpaert J V, Van Assche J A and Luijtens K 1992 The growth of the extramatrical mycelium of ectomycorrhizal fungi and the growth response of Pinus sylvestris L. New Phytol. 120, 127–135.

    Article  Google Scholar 

  • Connell J H 1978 Diversity in tropical rain forests and coral reefs: high diversity of trees and corals is maintained only in a nonequi-librium state. Science 199, 1307–1310.

    Article  Google Scholar 

  • Cooke R C and Rayner A D M 1984 Ecology of saprobic fungi. Longman, London. 415p.

    Google Scholar 

  • Dahlberg A and Stenlid J 1990 Population structure and dynamics in Suillus bovinus as indicated by spatial distribution of clones. New Phytol. 115, 487–483.

    Article  Google Scholar 

  • Danielson R M 1984 Ectomycorrhizal associations of jack pine in northeastern Alberta. Can. J. Bot. 62, 932–939.

    Article  Google Scholar 

  • Deacon J W, Donaldson S J and Last F T 1983 Sequences and interactions of mycorrhizal fungi on birch. Plant and Soil 71, 257–262.

    Article  Google Scholar 

  • Deacon J W and Fleming L V 1992 Interactions of ectomycorrhizal fungi. In Mycorrhizal Functioning an Integrative Plant-Fungal Process. Ed. M F Allen. pp 249–300. Chapman and Hall, New York.

    Google Scholar 

  • Dighton J, Poskitt J M and Howard D M 1986 Changes in occurrence of basidiomycete fruit bodies during forest stand development: with special reference to mycorrhizal species. Trans. Br. Mycol. Soc. 87, 163–171.

    Article  Google Scholar 

  • Dighton J, Thomas E D and Latter P M 1987 Interactions between tree roots, mycorrhizas, a saprophytic fungus and the decomposition of organic substrates in a microcosm. Biol. Fert. Soils 4, 145–150.

    Article  Google Scholar 

  • Duchesne L C, Peterson R L and Ellis B E 1988 Pine root exudate stimulates the synthesis of antifungal compounds by the ectomycorrhizal fungus Paxillus involutes. New Phytol. 108, 471–476.

    Article  CAS  Google Scholar 

  • Finlay R D, FrostegÃ¥rd Ã… and Sonnerfeldt A-M 1992 Utilization of organic and inorganic nitrogen sources by ectomycorrhizal fungi in pure culture and in symbiosis with Pinus contorta Doug, ex Loud. New Phytol. 120, 105–115.

    Article  Google Scholar 

  • Fleming L V 1983 Succession of mycorrhizal fungi on birch: infection of seedlings planted around mature trees. Plant and Soil 71, 263–267.

    Article  Google Scholar 

  • Fleming L V 1984 Effects of soil trenching and coring on the formation of ectomycorrhizas on birch seedlings grown around mature trees. New Phytol. 98, 143–153.

    Article  Google Scholar 

  • Fleming L V 1985 Experimental study of sequences of ectomycorrhizal fungi on birch (Betula sp) seedling root systems. Soil Biol. Biochem. 17, 591–600.

    Article  Google Scholar 

  • Fleming L V, Deacon J W and Last F W 1986 Ectomycorrhizal succession in a Scottish birch wood. In Physiological and Genetical Aspects of Mycorrhizae. Eds. V Gianinazzi-Pearson and S Gianinazzi. pp 259–264. INRA, Paris.

    Google Scholar 

  • Fogel R 1985 Roots as primary producers in below-ground ecosystems. In Ecological Interactions in Soil, Plants, Microbes, and Animals. Eds. A H Fitter, D Atkinson, D J Read and M B Usher. pp 23–36. Blackwell Scientific Publ., Oxford.

    Google Scholar 

  • Ford E D, Mason P A and Pelham J 1980 Spatial patterns of sporophore distribution around a young birch tree in three successive years. Trans. Br. Mycol. Soc. 75, 287–296.

    Article  Google Scholar 

  • Fox F M 1983 Role of basidiospores as inocula of mycorrhizal fungi of birch. Plant rand Soil 71, 269–273.

    Article  Google Scholar 

  • Fries N and Swedjemark G 198 Sporophagy in Hymenomycetes. Exp. Mycol. 9, 74–79.

    Google Scholar 

  • Garbaye J and Bowen G D 1989 Stimulation of ectomycorrhizal infection of Pinus radiata by some microorganisms associated with the mantle of ectomycorrhizas. New Phytol. 112, 383–388.

    Article  Google Scholar 

  • Garbaye J and Duponnois R 1992 Specificity and function of myc-orrhization helper bacteria (MHB) associated with Pseudotsuga menziesii-Laccaria laccata symbiosis. Symbiosis 14, 335–344.

    Google Scholar 

  • Gardes M and Bruns T D 1993 ITS primers with enhanced specificity for basidiomycetes — application to the identification of mycorrhizae and rusts. Mol. Ecol. 2, 113–118.

    Article  PubMed  CAS  Google Scholar 

  • Gardes M, White T J, Fortin J, Bruns T D and Taylor J W 1991 Identification of indigenous and introduced symbiotic fungi in ectomycorrhizae by amplification of nuclear and mitochondrial ribosomal DNA. Can. J. Bot. 69, 180–190.

    Article  CAS  Google Scholar 

  • Gibson F and Deacon J W 1988 Experimental study of establishment of ectomycorrhizas in different regions of birch root systems. Trans. Br Mycol. Soc. 91, 239–251.

    Article  Google Scholar 

  • Gibson F and Deacon J W 1990 Establishment of ectomycorrhizas in asceptic culture: effects of glucose, nitrogen and phosphorus in relation to successions. Mycol. Res. 94, 166–172.

    Article  Google Scholar 

  • Gill M and Steglich W 1987 Pigments of fungi (Macromycetes). In Progress in the Chemistry of Organic Natural Products. Vol. 51. Eds. W Herz, H Grisebach, G W Kerby and C Tamm. pp 1–317. Springer Verlag, New York.

    Google Scholar 

  • Giltrap N J 1982 Production of polyphenol oxidases by ectomycorrhizal fungi with special reference to Lactarius spp. Trans. Br Mycol. Soc. 78, 75–81.

    Article  CAS  Google Scholar 

  • Giltrap N J and Lewis D H 1982 Catabolite repression of the synthesis of pectin-degrading enzymes Suillus luteus (L. ex Fr.) 5. F. Gray and Heboloma oculatum Brunchet. New Phytol. 90, 485–493.

    Article  CAS  Google Scholar 

  • Griffith N T and Barnett H L 1967 Mycoparasitism by basidiomycetes in culture. Mycologia 59, 149–154.

    Article  PubMed  CAS  Google Scholar 

  • Grub P J 1977 The maintenance of species-richness in plant communities: the importance of the regeneration niche. Biol. Rev. 52, 107–145.

    Article  Google Scholar 

  • Harvey A E, Jurgensen M F and Larsen M J 1978 Seasonal distribution of ectomycorrhizae in mature Douglas-fir/Larch forest soil in Western Montana. For. Sci. 24, 203–208.

    Google Scholar 

  • Hendrick R L and Pregitzer K 51992 The demography of fine roots in a northern hardwood forest. Ecology 73, 1094–1104.

    Article  Google Scholar 

  • Ho I and Zak B 1979 Acid phosphatase activity of six ectomycorrhizal fungi. Can. J. Bot. 57, 1203–1205.

    Article  CAS  Google Scholar 

  • Hubbell S P 1979 Tree dispersion, abundance, and diversity in a tropical dry forest that trees are clumped, not spaced, alters concepts of the organization and dynamics. Science 203, 1299–1309.

    Article  PubMed  CAS  Google Scholar 

  • Krywolap G N, Grand L F and Casida L E J 1964 Natural occurrence of an antibiotic n the mycorrhizal fungus Cenococcum graniforme. Can. J. Microbiol. 10, 323–328.

    Article  PubMed  CAS  Google Scholar 

  • Last F T, Mason P A, Wilson J and Deacon J W 1983 Fine roots and sheathing mycorrhizas: their formation, function and dynamics. Plant and Soil 71, 9–21.

    Article  Google Scholar 

  • Lundeberg G 1970 Utilisation of various nitrogen sources, in particular bound nitrogen, by mycorrhizal fungi. Stud. For. Suec. 79, 1–95.

    Google Scholar 

  • Lussenhop J and Fogel R 1993 Observing soil biota in situ. Geoderma 56, 25–36.

    Article  Google Scholar 

  • Malajczuk N and Hingston F J 1981 Ectomycorrhizae associated with Jarrah. Aust. J. Bot. 29, 453–462.

    Article  Google Scholar 

  • Marks G C and Foster R C 1967 Succession of mycorrhizal associations on individual roots of radiata pine. Aust. For. 31, 193–201.

    Google Scholar 

  • Marx D H 1973 Mycorrhizae and feeder root diseases. In Ectomycorrhizae their Ecology and Physiology. Eds. G C Marks and T T Kozlowski. pp 351–382. Academic Press, New York.

    Google Scholar 

  • Mason P A, Last F T, Pelham J and Ingleby K 1982 Ecology of some fungi associated with an ageing stand of birches (Betula pendula and B. pubescens). For. Ecol. Manage. 4, 19–39.

    Article  Google Scholar 

  • Mason P A, Last F T, Wilson J, Deacon J W, Fleming L V and Fox F M 1987 Fruiting and successions of ectomycorrhizal fungi. In Fungal Infection of Plants: Symposium of the British Mycologi-cal Society. Eds. G F Pegg and P G Ayres. pp 253–268. Cambridge Univ. Press, Cambridge.

    Google Scholar 

  • Mason P A, Wilson J, Last F T and Walker C 1983 The concept of succession in relation to the spread of sheathing mycorrhizal fungi on inoculated tree seedlings growing in unsterile soils. Plant and Soil 71, 247–256.

    Article  Google Scholar 

  • McElhinney C and Mitchell D T 1993 Phosphatase activity of four ectomycorrhizal fungi found in a Sitka spruce-Japaneses larch plantation in Ireland. Mycol. Res. 97, 725–732.

    Article  CAS  Google Scholar 

  • Miller S L and Allen E B 1992 Mycorrhizae, nutrient translocation, and interactions between plants. In Mycorrhizal Functioning an Integrative Plant-Fungal Process. Ed. M F Allen. pp 301–332. Chapman and Hall, New York.

    Google Scholar 

  • Molina R, Massicotte H and Trappe J M 1992 Specificity phenomena in mycorrhizal symbioses: Community-Ecological consequences and practical implications. In Mycorrhizal Functioning an Integrative Plant-Fungal Process. Ed. M F Allen. pp 357–423. Chapman and Hall, New York.

    Google Scholar 

  • Murakami Y 1987 Spatial distribution of Russula species in Cas-tanopsis cuspidata forest. Trans. Br. Mycol. Soc. 89, 187–193.

    Article  Google Scholar 

  • Newell K 1984 Interaction between two decomposer basidiomycetes and a collembolan under Sitka spruce: distribution, abundance and selective grazing. Soil Biol. Biochem. 16, 227–233.

    Article  Google Scholar 

  • Newell K 1984 Interaction between two decomposer basidiomycetes and a collembolan under Sitka spruce: grazing and its potential effects on fungal distribution and litter decomposition. Soil Biol. Biochem. 16, 235–239.

    Article  Google Scholar 

  • Parkinson D, Visser S and Whittaker J B 1979 Effects of collembolan grazing on fungal colonization of leaf litter. Soil Biol. Biochem. 11, 529–535.

    Article  Google Scholar 

  • Pickett 5 T A 1980 Non-equilibrium coexistence of plants. Bull. Torrey Bot. Club 107, 238–248.

    Article  Google Scholar 

  • Pugh G J F and Boddy L 1988 A view of disturbance and life strategies in fungi. Proc. R. Soc. Edinburgh 94B, 3–11.

    Google Scholar 

  • Rayner A D M and Boddy L 1988 Fungal decomposition of wood. Its biology and ecology. Wiley and Sons, New York. 587 p.

    Google Scholar 

  • Rayner A D M, Boddy L and Dowson C G 1987 Temporary parasitism of Coriolus spp. by Lenzites betulina: a strategy for domain capture in wood decay fungi. FEMS Microbiol. Ecol. 45, 53–58.

    Article  Google Scholar 

  • Read D J 1991 Mycorrhizas in ecosystems. Experientia 47, 376–391.

    Article  Google Scholar 

  • Read D J 1992 The mycorrhizal mycelium. In Mycorrhizal Functioning an Integrative Plant-Fungal Process. Ed. M F Allen. pp 102–133. Chapman and Hall, New York.

    Google Scholar 

  • Richardson M J 1970 Studies on Russula emetica and other agarics in a scots pine plantation Trans. Br. Mycol. Soc. 55, 217–229.

    Article  Google Scholar 

  • Sagara N 1992 Experimental disturbances and epigeous fungi. In The fungal Community: Its Organization and Role in the Ecosystem. (2nd ed.). Eds. G C Carrol and D T Wicklow. pp 427–454. Marcel Dekker, New York.

    Google Scholar 

  • Sale P F 1977 Maintenance of high diversity in coral reef fish communities. Am. Nat. 111, 337–359.

    Article  Google Scholar 

  • Shaw P J A 1988 A consistent hierarchy in the fungal feeding preferences of the Collembola Onychiurus armatus. Pedobiologia 31, 179–187.

    Google Scholar 

  • Simon L, Bousquet J, Levesque R C and LaLonde M 1993 Origin and diversification of endomycorrhizal fungi and coincidence with vascular land plants. Nature 363, 67–69.

    Article  Google Scholar 

  • Singer R 1986 The Agaricales in Modern Taxonomy, 4th. ed, Koeltz Sc. Books, Koenigstein. 981 p.

    Google Scholar 

  • Slankis V 1973 Hormonal relationships in mycorrhizal development. In Ectomycorrhizae Their Ecology and Physiology. Eds. G C Marks and T T Kozlowski. pp 232–298. Academic Press, New York.

    Google Scholar 

  • Smucker A J M 1990 Quantification of root dynamics in agroeco-logical systems. Remote Sensing Rev. 5, 237–248.

    Article  Google Scholar 

  • Szaniszlo P J, Powell P E, Reid C P P and Cline G R 1981 Production of hydroxamate siderophore iron chelators by ectomycorrhizal fungi. Mycologia 73, 1158–1174.

    Article  CAS  Google Scholar 

  • Termorshuizen A J 1991 Succession of mycorrhizal fungi in stands of Pinus sylvestris in the Netherlands. J. Veg. Sci. 2, 555–564.

    Article  Google Scholar 

  • Thorn R G and Barron G L 1984 Carnivourous mushrooms. Science 224, 76–78.

    Article  PubMed  CAS  Google Scholar 

  • Trappe J M 1977 Selection of fungi for ectomycorrhizal inoculation in nurseries. Ann. Rev. Phytopath. 15, 203–22.

    Article  Google Scholar 

  • Trojanowski J, Haider K and Hüttermann A 1984 Decomposition of 14C-labelled lignin, holocellulose, and lignocellose by mycorrhizal fungi. Arch. Microbiol. 139, 202–206.

    Article  CAS  Google Scholar 

  • Väre H 1989 Influence of decaying birch logs to Scots Pine mycorrhizae at clear-cutted ploughed sites in Northern Finland. Agric. Ecosyst. Environ. 28, 539–55.

    Article  Google Scholar 

  • Vogt K A, Bloomfield J, Ammirati J F and Ammirati S R 1992 Sporocarp production by basidiomycetes with emphasis on forest ecosystems. In The Fungal Community its Organization and Role in the Ecosystem. (2nd ed.). Eds. G C Carrol and D T Wicklow. pp 563–581. Marcel Dekker, New York.

    Google Scholar 

  • Zak B and Marx D H 1964 Isolation of mycorrhizal fungi from roots of individual slash pines. For. Sci. 10, 214

    Google Scholar 

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  1. Division of Entomology, Plant and Soil microbiology, Department of Environmental Science, Policy, Management, University of California, Berkeley, CA, 94720, USA

    Thomas D. Bruns

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H. P. Collins G. P. Robertson M. J. Klug

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Bruns, T.D. (1995). Thoughts on the processes that maintain local species diversity of ectomycorrhizal fungi. In: Collins, H.P., Robertson, G.P., Klug, M.J. (eds) The Significance and Regulation of Soil Biodiversity. Developments in Plant and Soil Sciences, vol 63. Springer, Dordrecht. https://doi.org/10.1007/978-94-011-0479-1_5

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  • DOI: https://doi.org/10.1007/978-94-011-0479-1_5

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