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Noogoora burr
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Worldwide, Noogoora burr is an annual weed of 11 major agricultural
crops in 28 countries, and is listed one of the 10 most noxious
weeds in the USA (Hocking and Liddle, 1995). It is a major
problem to the livestock industry because it competes with
palatable plants, seedlings are toxic to stock, burrs reduce
wool values and it poses quarantine issues. In far northern
Australia it continues to invade previously un-infested catchments
and is currently perceived to be a major threat by pastoralists
and government agencies. Noogoora burr is a weed across northern
Australia, mostly of riparian areas.
Background
Noogoora burr was one of the first weeds to be systematically
targeted by biological control and there were two major phases
in the Australian program: 1929-1940; 1953-1975. Three agents
have been released: a seed-feeding fly in the 1930s, and two
stem-borers in the 1960s. None have resulted in significant
impact. A fourth insect, a gall-forming moth (Epiblemma
strenuana) was released against parthenium in 1982 and
also attacks Noogoora burr, on which it causes some damage.
However, Noogoora burr infestations along eastern Australia
have been largely brought under control by the rust Puccinia
xanthii which was accidentally or illegally introduced
into Australia in 1975. The rust fungus though has not controlled
infestations in the far north (including the Northern Territory
and Western Australia).
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Noogoora bur along Victoria river
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An eradication program was terminated in the Kimberley in
the early 1990's, and the remaining populations contained
within a quarantine zone. NT Department of Infrastructure,
Planning and Environment have also considered Noogoora burr
to be an important weed and contracted CSIRO in 1999 to review
past biological control attempts and to determine the potential
of renewing it. This report highlighted that the best bet
for successful biological control is to find a rust strain
that is better suited to climatic conditions in northern Australia
(especially warmer summer minima).
Enhancing biocontrol in northern Australia
Achievements of 2006-08 project
Field surveys for exotic isolates of Puccinia xanthii were undertaken in 2007 in Venezuela, Mexico and Dominican Republic, areas that climatically match those of northern Australia where the rust fungus has not been highly effective (van Klinken & Julien, 2003). Rust-infected material from 12 sites in Dominican Republic and Mexico was imported into the CSIRO Black Mountain Containment Facility in Canberra.
Pathogenicity tests revealed that Noogoora burr and other Xanthium spp. from Australia were resistant to these exotic rust isolates. In contrast, plants inoculated with Australian rust isolates developed disease symptoms. This was expected based on a previous study which showed that Xanthium spp. comprised in the ‘Noogoora burr complex’ were susceptible to an Australian isolate of P. xanthii.
Closer examination of Xanthium specimens collected in the Dominican Republic and Mexico confirmed that they were morphologically and genetically different (based on chloroplast and ribosomal DNA sequence data) to Australian accessions of Noogoora burr and other Xanthium spp.

Noogoora burr rust fungus,
Puccinia xanthii
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A diagnostic microsatellite marker to differentiate between exotic and Australian rust isolates was successfully developed to provide a tool for monitoring exotic isolates, should any be released in Australia. Primers were designed to amplify eight microsatellites (Simple Sequence Repeats) DNA loci isolated and characterised from genomic DNA of P. xanthii. Genetic variation at these loci was observed across 29 single-telium isolates from Australia, Hungary, Brazil, Argentina, Mexico and Dominican Republic. Allelic variation at some loci was useful in discriminating between isolates from Australia and tropical America.
Baseline data on Noogoora burr populations and prevalence of biocontrol agents (P. xanthii and the moth Epiblemma strenuana) were collected by collaborators from the Department of Natural Resources, Environment and the Arts (NRETA) at sites on three river systems in the Northern Territory and northern Western Australia. This data will be essential to assess the impact of additional isolates of P. xanthii, should any be released in the future in Australia.
Conclusion
Genetic differences between Xanthium accessions from tropical America and Australian Noogoora burr accessions most likely explain why the latter were not infected by the tropical American isolates of P. xanthii.
A more extensive follow-up project is required to deliver on the original goal of introducing additional isolates of P. xanthii better adapted to the climate of tropical northern Australia. The establishment of an outdoor experimental garden consisting of northern Australian accessions of Noogoora burr in tropical America would be required to source pathogenic rust isolates.
Key People
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Dr Rieks
van Klinken
CSIRO Entomology
Long Pocket Laboratories
120 Meiers Road
Indooroopilly QLD 4068
AUSTRALIA
Ph: +61 7 3214 2761
Fax: +61 7 3214 2885
Email: firstname.lastname@csiro.au
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Dr Louise
Morin
CSIRO Entomology
GPO Box 1700
Canberra ACT 2601
AUSTRALIA
Ph: +61 2 6246 4355
Fax: +61 2 6246 4362
Email: firstname.lastname@csiro.au
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Collaborators
DAFWA - Department of Agriculture and food, Western Australia
Australian Government, DAFF – Department of Agriculture, Fisheries and Forestry
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