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Phenotypic variation in a clonal lineage of two Phytophthora cinnamomi populations from Western Australia

Published online by Cambridge University Press:  16 October 2001

Daniel HÜBERLI
Affiliation:
School of Biological Sciences and Biotechnology, Murdoch University, Perth WA 6150, Australia. E-mail: g-hardy@central.murdoch.edu.au
Inez C. TOMMERUP
Affiliation:
CSIRO, Forestry and Forest Products, PO Box 5, Wembley WA 6913, Australia.
Mark P. DOBROWOLSKI
Affiliation:
School of Biological Sciences and Biotechnology, Murdoch University, Perth WA 6150, Australia. E-mail: g-hardy@central.murdoch.edu.au
Michael C. CALVER
Affiliation:
School of Biological Sciences and Biotechnology, Murdoch University, Perth WA 6150, Australia. E-mail: g-hardy@central.murdoch.edu.au
Giles E. St J. HARDY
Affiliation:
School of Biological Sciences and Biotechnology, Murdoch University, Perth WA 6150, Australia. E-mail: g-hardy@central.murdoch.edu.au
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Abstract

Seventy-three isolates of Phytophthora cinnamomi were collected from diseased Eucalyptus marginata (jarrah) and Corymbia calophylla (marri) trees in two forest communities in the southwest of Western Australia. Both populations of P. cinnamomi were examined for phenotypic and genotypic variation. Microsatellite DNA analysis showed that all isolates were of the same clonal lineage. We show, for the first time for P. cinnamomi, that morphological and pathogenic variation between populations of the clonal lineage are very broad and continuous. The phenotypes examined included growth rates and colony morphology on potato dextrose agar at different temperatures, sporangial and gametangial morphology, ability to form lesions in detached jarrah and marri stems, and ability to cause deaths of clonal jarrah plants in a glasshouse trial. Phenotype variation was derived asexually. All phenotypes investigated varied independently from one another. Cluster analysis of 24 morphological and pathogenicity phenotypes identified two main clusters of isolates corresponding to each population. The ability to cause deaths in both populations ranged from killing all plants within 59 d to plants being symptomless 182 d after inoculation.

Type
Research Article
Copyright
© The British Mycological Society 2001

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