Oecologia

, Volume 85, Issue 2, pp 178–184 | Cite as

Population structure and responses to disturbance of the basidiomycete Resinicium bicolor

  • J. J. H. Kirby
  • J. Stenlid
  • O. Holdenrieder
Original Papers

Summary

Resinicium bicolor (Alb. & Schw. ex Fr.) Parm. [=Odontia bicolor (Alb. & Schw. ex Fr.) Bres.] is an outcrossing resupinate basidiomycete associated with root and butt rots of trees, but is itself only very weakly pathogenic. The distribution of genets among every spruce stump in a 70-year-old 1250 m2 spruce stand was analysed using somatic incompatibility testing. R. bicolor was present on 40% of 8-to 10-year-old stumps. Nineteen genets were found occupying 32 stumps; yielding probabilities of colonisation following establishment by basidiospores of 0.20–0.24 and by mycelial extension or dispersal of 0.16–0.20. The probability of colonisation decreased with increasing distance from a point of establishment. R. bicolor responded to both enrichment and destructive disturbances by the formation of an extensive cord system which enabled it to colonise discontinuously distributed resources and to overgrow fungi adjacent to it in a single resource unit, including Heterobasidion annosum.

Key words

Population structure Disturbance Resinicium bicolor Heterobasidion annosum Biological control 

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References

  1. Boddy L, Rayner ADM (1988) Fungal decomposition of wood. John Wiley, Chichester, pp 587Google Scholar
  2. Chamuris GP, Falk SP (1987) The population structure of Peniophora rufa in an aspen plantation. Mycologia 79:451–457Google Scholar
  3. Childs TW (1963) Poria weirii root rot. Phytopathology 53:1124–1127Google Scholar
  4. Dahlberg A, Stenlid J (1990) Population structure and dynamics in Suillus bovinus as reflected by spatial distributions of fungal clones. New Phytol 115:487–493Google Scholar
  5. Dickman A, Cook S (1989) Fire and fungus in a mountain hemlock forest. Can J Bot 67:2005–2016Google Scholar
  6. Domanski S (1976) Resinicium bicolor in Poland. Mem New York Bot Garden 28:58–66Google Scholar
  7. Dowson CG, Springham P, Rayner ADM, Boddy L (1989) Resource relationships of foraging mycelial systems of Phanerochaete velutina and Hypholoma fasciculare in soil. New Phytol 111:501–509Google Scholar
  8. Greig-Smith P (1983) Quantitative plant ecology. Blackwell, Oxford, pp 359Google Scholar
  9. Hallaksela A-M (1984) Causal agents of butt rot in Norway spruce in Southern Finland. Silv Fenn 18:237–243Google Scholar
  10. Harrington TC, Worrall JJ, Rizzo DM (1989). Root and butt rots and other disturbance agents in montane spruce-fir forests of New Hampshire. In: Morrison DJ (ed) Proceedings of the seventh international conference on root and butt rots. Forestry Canada, Victoria British Columbia, pp 257–266Google Scholar
  11. Hengeveld R (1989) Dynamics of biological invasions. Chapman and Hall, London, pp 160Google Scholar
  12. Holdenrieder O (1984) Untersuchungen zur biologischen Bekämpfung von Heterobasidion annosum an Fichte (Picea abies) mit antagonistischen Pilzen. Eur J For Path 14:137–153Google Scholar
  13. Hood IA, Sandberg CJ (1989) Changes in soil populations of Armillaria species following felling and burning of indigenous forest in the Bay of Plenty, New Zealand. In: Morrison DJ (ed) Proceedings of the seventh international conference on root and butt rots. Forestry Canada, Victoria, British Columbia pp 288–296Google Scholar
  14. Hutchings MJ (1986) The structure of plant populations. In: Crawley MJ (ed) Plant ecology. Blackwell, Oxford, pp 97–136Google Scholar
  15. Hutchings MJ, Slade AJ (1988) Morphological plasticity, foraging and integration in clonal perennial herbs. In: Davy AJ, Hutchings MJ, Watkinson AR (eds) Plant population ecology. Blackwell, Oxford, pp 83–109Google Scholar
  16. Kile GA (1983) Identification of genotypes and the clonal development of Armillaria luteobubalina in eucalypt forests. Aust J Bot 31:657–671Google Scholar
  17. Kile GA (1986) Genotypes of Armillaria in wet sclerophyll eucalypt forest in Tasmania. Trans Brit mycol Soc 87:312–314Google Scholar
  18. Korhonen K (1978) Interfertility and clonal size in the Armillaria mellea complex. Karstenia 18:31–42Google Scholar
  19. Lussenhop J (1981) Analysis of microfungal component communities. In: Wicklow DT, Carroll GC (eds) The fungal community: its organization and roles in the ecosystem. Marcel Dekker, New York, pp 37–46Google Scholar
  20. Nobles MK (1964) Identification of cultures of wood-inhabiting hymenomycetes. Can J Bot 43:1097–1139Google Scholar
  21. Pearce MH, Malajczuk N (1990) Inoculation of Eucalyptus diversicolor thinning stumps with wood decay fungi for control of Armillaria luteobubalina. Mycol Res 94:32–37Google Scholar
  22. Rayner ADM, Todd N (1982) Population structure in wood-decomposing basidiomycetes. In: Frankland JC, Hedger JN, Swift MJ (eds) Decomposer Basidiomycetes: their biology and ecology. Cambridge University Press, Cambridge, pp 109–128Google Scholar
  23. Schönhar S (1973) Zur Ausbreitung von Fomes annosus und anderer Rotfäulepilze in Fichtenbeständen 2. Generation. Mitt Ver Forstl Standortsk Forstpflanzenz 22:3–8Google Scholar
  24. Schönhar S (1988) Zur Ausbreitung von Heterobasidion annosum in Fichtenbeständen. Forst und Holz 7:156–158Google Scholar
  25. Shaw CG III (1989) Root disease threat minimal in young stands of western hemlock and Sitka spruce in Southeastern Alaska. Plant Disease 73:573–577Google Scholar
  26. Siepmann R (1971) Über Odontia bicolor (Alb. & Schw.) Quel. und Amylostereum areolatum (Fr.) Boidin, zwei stammfäuleerregende Basidiomyceten in lebenden Fichten (Picea abies). Fortwiss Centralblatt 90:337–340Google Scholar
  27. Siepmann R (1976) Uber die Infektion von Fichtenwurzeln (Picea abies Karst.) durch Fomes annosus (Fr.) Cke. Eur J For Path 6:342–347Google Scholar
  28. Siepmann R (1981a) Ein Beitrag zur Regeneration und zur Infektion von Fichtenwurzeln (Picea abies Karst.) durch Basidio-und Ascomyceten. Eur J For Path 11:59–66Google Scholar
  29. Siepmann R (1981b) Ein Beitrag zur Regeneration und zur Infektion von Douglasienwurzeln [Pseudotsuga menziesii (Mirb.) Franco] durch Pilze aus dem Boden. Eur J For Path 11:162–169Google Scholar
  30. Stenlid J (1985) Population structure of Heterobasidion annosum as determined by somatic incompatibility, sexual incompatibility and isoenzyme patterns. Can J Bot 63:2268–2273Google Scholar
  31. Stenlid J (1987) Controlling and predicting the spread of Heterobasidion annosum from infected trees and stumps of Picea abies. Scand J For Res 2:187–198Google Scholar
  32. Swift MJ (1976) Species diversity and the structure of microbial communities in terrestrial habitats. In: Anderson JM, Macfadyen A (eds) The role of terrestrial and aquatic organisms in decomposition processes. Blackwell, Oxford, pp 185–222Google Scholar
  33. Thompson W, Rayner ADM (1982) Spatial structure of a population of Tricholomopsis platyphylla in a woodland site. New Phytol 92:103–114Google Scholar
  34. Thompson W, Boddy L (1983) Decomposition of suppressed oak trees in even-aged plantations. II. Colonisation of tree roots by cord and rhizomorph producing basidiomycetes. New Phytol 93:277–291Google Scholar

Copyright information

© Springer-Verlag 1990

Authors and Affiliations

  • J. J. H. Kirby
    • 1
  • J. Stenlid
    • 1
  • O. Holdenrieder
    • 1
  1. 1.Department of Forest Mycology and PathologySwedish University of Agricultural SciencesUppsalaSweden

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