Skip to main content
Log in

The contributions of mycorrhizal fungi to the determination of plant community structure

  • Published:
Plant and Soil Aims and scope Submit manuscript

Abstract

While it is now widely accepted, even by ecologists, that most plants in the majority of ecosystems are infected by mycorrhizal fungi, few experiments have been designed to investigate the function of the mutualism at the community level. Those involved with mycorrhizal research have been largely preoccupied with questions of the mineral, particularly phosphorus, nutrition of individual plants, while plant community ecologists have too often found it convenient, even when acknowledging the presence of infection, to ignore its possible function in the ecosystem.

This presentation examines a selected number of seminal papers written by plant community ecologists and highlights some of ‘the most striking mysteries’ which they reveal. It describes experiments designed to determine whether knowledge of the presence and activity of the mycorrhizal mycelium can help us to unravel the ‘mysteries’ which they define.

It is revealed that by having direct adverse effects upon seedlings of many ‘r’ selected species, while at the same time being beneficial, if not essential, to those that are ‘K’ selected, the activities of the mycelium of VA fungi have a direct bearing upon community composition. The extent to which ‘turf compatibility’ is actually a reflection of the compatibility of plant species with the VA mycorrhizal mycelium is discussed and the possible role of the mycelium in consigning some species to the ruderal habit is considered.

It is concluded that those attempting scientifically to understand, or managerially to manipulate, plant communities, without recognizing the role of the mycorrhizal mycelium, do so at their peril, and it is recommended that scientists involved in research on mycorrhiza extend their vision beyond the limited horizons which are currently so often defined by considerations of the phosphorus nutrition of individual host plants.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • AbbottL K and RobsonA D 1985 Formation of external hyphae in soil by four species of vesicular-arbuscular mycorrhizal fungi. New Phytol. 99, 245–244.

    Article  Google Scholar 

  • AbbottL K, RobsonA D and DeBoerG 1984 The effect of phosphorus on the formation of hyphae in soil by the vesicular-arbuscular mycorrhizal fungus Glomus fasciculatum. New Phytol. 97, 437–446.

    Article  CAS  Google Scholar 

  • AbuzinadahR A and ReadD J 1986a 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 

  • AbuzinadahR A and ReadD J 1986b The role of proteins in the nitrogen nutrition of ectomycorrhizal plants. III. Protein utilization by Betula, Picea in mycorrhizal association with Hebeloma crustuliniforme. New Phytol. 103, 507–514.

    Article  CAS  Google Scholar 

  • AbuzinadahR A and ReadD J 1989a The role of proteins in the nitrogen nutrition of ectomycorrhizal plants. IV. The utilization of peptides by birch (Betula pendula L.) infected with different mycorrhizal fungi. New Phytol. 112, 55–60.

    Article  CAS  Google Scholar 

  • AbuzinadahR A and ReadD J 1989b The role of proteins in the nitrogen nutrition of ectomycorrhizal plants. V. Nitrogen transfer in birch (Betula pendula) grown in association with mycorrhizal and non-mycorrhizal fungi. New Phytol. 112, 61–68.

    Article  CAS  Google Scholar 

  • AllenE B and AllenM F 1980 Natural re-establishment of vesicular-arbuscular mycorrhizae following stripmine reclamation in Wyoming. J. Appl. Ecol. 17, 139–147.

    Article  Google Scholar 

  • AllenM F, AllenE B and FrieseC G 1989 Responses of the non-mycotrophic plant Salsola kali to invasion by vesicular-arbuscular mycorrhizal fungi. New Phytol. 111, 45–49.

    Article  Google Scholar 

  • Amaranthus M P, Molina R and Perry D A 1990 Soil organisms, root growth and forest regeneration. Proc. Soc. Amer. for Spokane Washington. pp 89–93.

  • BorchersS L and PerryD A 1990 Growth and ectomycorrhiza formation of Douglas-fir seedlings grown in soils collected at different distances from pioneering hardwoods in southwest Oregon clear-cuts Can. J. For. Res. 20, 712–721.

    Google Scholar 

  • BuwaldaJ G 1980 Growth of a clover-rye grass association with vesicular-arbuscular mycorrhizas. N. Z. J. Agric. Res. 23, 379–383.

    Google Scholar 

  • CarletonT J and ReadD J 1991 Ectomycorrhizas and nutrient transfer in conifer-feathermoss ecosystems. Can. J. Bot. 69, 778–785.

    Google Scholar 

  • ChilversG A and PryorL D 1965 The structure of eucalypt mycorrhizas. Aust. J. Bot. 13, 245–261.

    Google Scholar 

  • CouttsM P and NicollB C 1990a Growth and survival of shoots, roots and mycorrhizal mycelium in clonal Sitka spruce during the first growing season after planting. Can. J. For. Res. 20, 861–868.

    Google Scholar 

  • CouttsM P and NicollB C 1990b Waterlogging tolerance of roots of Sitka spruce clones and of strands from Thelephora terrestris mycorrhizas. Can. J. For. Res. 20, 1896–1899.

    Google Scholar 

  • CromackK, SollinsP, GransteinW C, SpeidelK, ToddA W, SpycherG, ChingY-Li and TodR L 1979 Calcium oxalate accumulation and soil weathering in mats of the hypogeous fungus Hysterangium crassum. Soil Biol. Biochem. 11, 463–468.

    Article  CAS  Google Scholar 

  • DahlbergA and StenlidJ 1990 Population structure and dynamics in Suillus bovinus as indicated by spatial distribution of fungal clones. New Phytol. 115, 487–493.

    Article  Google Scholar 

  • EntryJ A, RoseC L and CromackJrK 1991a Litter decomposition and nutrient release in ectomycorrhizal mat soils of a Douglas fir ecosystem Soil Biol. Biochem. 23, 285–290.

    Article  CAS  Google Scholar 

  • EntryJ A, DonnellyP K and CromackJrK 1991b Influence of ectomycorrhizal mat soils on lignin and cellulose degradation. Biol. Fert. Soils 11, 75–78.

    Article  CAS  Google Scholar 

  • FennerM 1978 A comparison of the abilities of colonizers and closed turf species to establish from seed in artificial swards. J. Ecol. 66, 953–965.

    Article  Google Scholar 

  • FinlayR D and ReadD J 1986a 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.

    Article  Google Scholar 

  • FinlayR D and ReadD J 1986b The structure and function of the vegetative mycelium of ectomycorrhizal plants. II. The uptake and distribution of phosphorus by mycelial strands inter-connecting host plants. New Phytol. 103, 157–165.

    Article  Google Scholar 

  • FitterA H 1977 Influence of mycorrhizal infection on competition for phosphorus and potassium by two grasses. New Phytol. 79, 19–25.

    Article  Google Scholar 

  • FlemingL 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 

  • GlennM G, ChewF S and WilliamsP H 1985 Hyphal penetration of Brassica (Cruciferae) roots by a vesicular-arbuscular mycorrhizal fungus. New Phytol. 99, 463–472.

    Article  Google Scholar 

  • GriffithsR, CaldwellB A, CromackJrK, CastellanoM A and MoritaR Y 1987 A study of the chemical and microbial variables in forest soils colonized with Hysterangium setchellii rhizomorphs. In Mycorrhizae in the Next Decade: Practical Applications and Research Priorities, Proc. 7th NACOM. Eds. D MSilva, L LHung and J HGraham. p 96. Institute of Food and Agricultural Science, University of Florida, Gainesville, Florida.

    Google Scholar 

  • GriffithsR P, CastellanoM A and CaldwellB A 1991 Hyphal mats formed by two ectomycorrhizal fungi and their association with Douglas-fir seedlings: A case study. Plant Soil 134, 255–259.

    Article  Google Scholar 

  • GrimeJ P 1979 Plant strategies and vegetation processes. John Wiley and Sons, New York. 222 p.

    Google Scholar 

  • GrimeJ P, MackeyJ M L, SillierS H and ReadD J 1987 Floristic diversity in a model system using experimental microcosms. Nature (London) 328, 420–422.

    Article  Google Scholar 

  • GrimeJ P, HodgsonJ G and HuntR 1988 Comparative plant ecology. A functional approach to common British species. Unwin and Hyman, London. 742 p.

    Google Scholar 

  • Grubb P J 1986 The ecology of establishment. In Ecology and Design in Landscape. Symp. Br. Ecol. Soc. 24. Eds. A D Bradshaw, D A Goode and E Thorpe. pp 83–97.

  • HallI T 1978 Effects of endomycorrhizas on the competitive abilities of white clover. N. Z. J. Agric. Res. 21, 509–515.

    Google Scholar 

  • HarleyJ L and SmithS E 1983 Mycorrhizal Symbiosis, Academic press, London. 483 p.

    Google Scholar 

  • HarleyJ L and HarleyE L 1987 Check list of mycorrhizas in the British flora. New Phytol. 105, 1–102.

    Article  Google Scholar 

  • HarveyA E, LarsenM J and JurgensenM F 1976 Distribution of ectomycorrhizae in a mature Douglas fir/larch forest system in Western Montana. For. Sci. 22, 393–398.

    Google Scholar 

  • HetrickB A D, KittD G and WilsonG T 1988 Mycorrhizal dependence and growth habit of warm-season and cool-season tallgrass prairie plants. Can. J. Bot. 66, 1376–1380.

    Google Scholar 

  • HetrickB A D, WilsonG W T and HartnettD C 1989 Relationship between mycorrhizal dependence and competitive ability of two tallgrass prairie grasses. Can. J. Bot. 67, 2608–2615.

    Article  Google Scholar 

  • JanosD P 1980 Mycorrhizae influence tropical succession. Biotropica 12, 56–64.

    Article  Google Scholar 

  • KoideR T and LuX 1991 Avena fatua L seed and seedling nutrient dynamics as influence by mycorrhizal infection of the maternal generation. Plant Cell. Env. 14, 931–939.

    Article  Google Scholar 

  • KoideR T, LiM, LewisJ and IrbyC 1988 Role of mycorrhizal infection in the growth and reproduction of wild US cultivated plants. I. Wild US cultivated oats. Oecologia 77, 537–549.

    Article  Google Scholar 

  • LewisJ D and KoideR T 1990 Phosphorus supply, mycorrhizal infection and plant offspring vigour. Functional Ecol. 4, 695–702.

    Article  Google Scholar 

  • MillerR M 1987 The ecology of vesicular-arbuscular mycorrhizal in grass and shrublands. In Ecophysiology of VA Mycorrhizal Plants. Ed. G RSafir. pp 135–170. CRC Press, Boca Raton, USA.

    Google Scholar 

  • MolinaR, MassicotteH and TrappeJ M 1991 Specificity phenomena in mycorrhizal symbioses: Community-ecological consequences and practical implications. In Mycorrhizal Functioning: An Integrative Plant-Fungal Process. Ed. M FAllen. pp 357–423. Chapman and Hall, New York.

    Google Scholar 

  • NewmanE I 1969 Resistance to water flow in soil and plant. I. Soil resistance in relation to amounts of root: theoretical estimates. J. Appl. Ecol. 6, 1–12.

    Article  Google Scholar 

  • NewtonA C and PigottD 1991 Mineral nutrition and mycorrhizal infection of oak and birch. I. Nutrient uptake and the development of mycorrhizal infection during seedling establishment. New Phytol. 17, 37–44.

    Article  Google Scholar 

  • OcampoJ A MartinJ and HaymanD S 1980 Influence of plant interactions on vesicular-arbuscular mycorrhizal infections. I. Host and non-host plants grown together. New Phytol. 84, 27–35.

    Article  Google Scholar 

  • OcampoJ A and HaymanD A 1981 Influence of plant interactions on vesicular-arbuscular mycorrhizal infections. II. Crop rotations and residual effects of non-host plants. New Phytol. 87, 333–334.

    Article  Google Scholar 

  • ParrishJ A D and Bazzaz 1985 Nutrient content of Abutilon theophrasti seeds and competitive ability of the resulting plants. Oecologia 65, 247–251.

    Article  Google Scholar 

  • PerssonH 1979 Fine-root production, mortality and decomposition in forest ecosystem. Vegetatio 41, 101–109.

    Article  Google Scholar 

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

    Article  Google Scholar 

  • ReadD J 1992 The mycorrhizal mycelium. In Mycorrhizal Functioning. An integrative plant-fungal process. Ed. MAllen. pp 102–133. Chapman and Hall, New York.

    Google Scholar 

  • ReadD J and BirchC P D 1988 The effects and implications of disturbance of mycorrhizal mycelial systems. Proc. R. Soc. Edinburgh 94B, 13–24.

    Google Scholar 

  • ReadD J, KouchekiH K and HodgsonJ 1976 Vesicular-arbuscular mycorrhiza in natural vegetation systems. I. The occurrence of infection. New Phytol. 77, 541–655.

    Article  Google Scholar 

  • ReadD J, FranicsR and FinlayR D 1985 Mycorrhizal mycelia and nutrient cycling in plant communities. In Ecological Interactions in Soil: Plants, Microbes and Animals. Eds. A HFitter, DAtkinson, D JRead and M BUsher. pp 193–217. British Ecological Society special Publication 4, Blackwell, Oxford.

    Google Scholar 

  • ReddellP and MalajczukN 1984 Formation of ectomycorrhizae by jarrah (Eucalyptus marginata Donn ex Smith) in litter and soil. Aust. J. Bot. 32, 435–444.

    Article  Google Scholar 

  • ReevesF B, WagnerD W, MoormanT and KielJ 1979 The role of endomycorrhizae in revegetation practises in the semi-arid west. I. A comparison of incidence of mycorrhizae in severely disturbed US natural environments. Am. J. Bot. 66, 1–13.

    Article  Google Scholar 

  • SandersF E and TinkerP B 1973 Phosphate flow into mycorrhizal roots. Pestic. Sci. 4, 385–395.

    CAS  Google Scholar 

  • Scherfose V 1990 Feinwurzelverterlung und Mycorrhizatypen von Pinus sylvestris in verschiedenen Bodentypen Berichte Forschungszentrum Wald ökosysteme. Univ. Göttingen, Reihe A Bd 62 166 p.

  • SylviaD M 1990 Distribution, structure and function of external hyphae of vesicular-arbuscular mycorrhizal fungi. In Rhizosphere dynamics Eds. J EBox, L CHammond. pp 144–167. Westview Press, Boulder, Co.

    Google Scholar 

  • TisdallJ M and OadesJ M 1979 Stabilization of soil aggregates by the root segments of rye grass. Aust. J. Soil Res. 17, 429–441.

    Article  Google Scholar 

  • TrappeJ M 1987 Phylogenetic and ecological aspects of mycotrophy in the angiosperms from an evolutionary standpoint. In Ecophysiology of VA Mycorrhizal plants. Ed. G RSafir. pp 2–25. CRC Press, Boca Raton, USA.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Francis, R., Read, D.J. The contributions of mycorrhizal fungi to the determination of plant community structure. Plant Soil 159, 11–25 (1994). https://doi.org/10.1007/BF00000091

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00000091

Key words

Navigation