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Letters to Nature
Nature 379, 63 - 66 (04 January 1996); doi:10.1038/379063a0

Evolution of extreme specialization within a lineage of ectomycorrhizal epiparasites

K. W. Cullings*, T. M. Szaro & T. D. Bruns

Department of Environmental Science, Policy, and Management, University of California, Berkeley, California 94720 USA
*Present address Department of Biology, San Francisco State University, California 94132, USA

MONOTROPES (Monotropoideae, Ericaceae) are achlorophyllous, epiparasitic plants that receive all of their fixed carbon from green plants through a common ectomycorrhizal association rather than by a direct parasitic connection (Fig. 1)1,2. Using molecular identification methods we show that some monotropes are highly specific in their fungal associations and at least one species, Pterosporo andromedea is specialized on a single species group within the genus Rhizopogon. Phylogenetic analysis of the Monotropoideae shows that specialization has been derived through narrowing of fungal associations within the lineage containing P. andromedea. High specificity is contrary to past predictions for the Monotropoideae and for plant communities in general, raising many questions about the roles of mycorrhizal specificity in ecosystem function.

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References
1. Björkman, E. Physiol. Plt. 13, 308−327 (1960).
2. Leake, J. R. New Phytol. 127, 171−216 (1994). | ISI |
3. Read, D. J. Experientia 47, 376−391 (1991). | ISI |
4. Malloch, D. W., Pirozynski, K. A. & Raven, P. H. Proc. natn. Acad. Sci. U.S.A. 77, 2113−2118 (1980).
5. Borowicz, V. A. & Juliano, S. A. Evol. Ecol. 5, 385−392 (1991).
6. Molina, R., Massicotte, H. & Trappe, J. M. in Mycorrhizal Functioning; An Integrative Plant-Fungal Process (ed. Allen, M. F.) 357−423 (Chapman and Hall, New York, 1992).
7. Van der Plank, J. E. Genetic and Molecular Basis of Plant Pathogenesis (Springer, New York, 1978).
8. Castellano, M. A. & Trappe, J. M. Mycologia 77, 499−502 (1985).
9. Bruns, T. D., Fogel, R., White, T. J. & Palmer, J. D. Nature 339, 140−142 (1989). | Article | PubMed | ChemPort |
10. Bruns, T. D. & Szaro, T. M. Molec. Biol. Evol. 9, 836−855 (1992). | PubMed | ChemPort |
11. Miller, S. I., Koo, C. D. & Molina, R. Can. J. Bot. 69, 516−532 (1991).
12. Bruns, T. D. Pl. Soil 170, 63−73 (1995). | ChemPort |
13. Natarajan, K., Mohan, V. & Ingelby, K. Soil Biol. Biochem. 24, 279−280 (1992). | Article |
14. Danielson, R. M. Can. J. Bot. 62, 932−939 (1984). | ISI |
15. Thompson, J. N. The Coevolutionary Process 1−376 (University of Chicago Press, 1994). | ChemPort |
16. Price, P. W. Evolutionary Biology of Parasites 1−237 (Princeton University Press, Princeton, NJ, 1980). | ChemPort |
17. Cullings, K. J. Evol. Biol. 7, 501−516 (1992).
18. Janzen, D. H. Evolution 34, 611−612 (1980). | ISI |
19. Molina, R. & Trappe, J. M. New Phytol. 126, 653−675 (1994).
20. Molina, R. & Trappe, J. M. Forest Sci. 28, 423−458 (1982). | ISI |
21. Finlay, R. D. New Phytol. 112, 185−192 (1989). | ChemPort |
22. Bruns, T. D. & Gardes, M. Molec. Ecol. 2, 233−242 (1993). | ChemPort |
23. Gardes, M. & Bruns, T. D. Molec. Ecol. 2, 113−118 (1993). | ChemPort |
24. Baura, G., Szaro, T. M. & Bruns, T. B. Mycologia 84, 592−597 (1992). | ChemPort |
25. Vilgalys, R. & Sun, B. L. Proc. natn. Acad. Sci. U.S.A. 91, 4599−4603 (1994). | ChemPort |
26. Kasuga, T., Woods, C., Woodward, S. & Mitchelson, K. Curr. Genet. 24, 433−436 (1993). | Article | PubMed | ChemPort |
27. Felsenstein, J. PHILIP (Computer program, Univ. Washington, Seattle, 1995).
28. Swofford, D. L. PAUP (Computer program, Smithsonian Institution, Washington, DC, 1993).
29. Molina, R. & Trappe, J. M. New Phytol. 90, 495−509 (1982).



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