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Pleiochaeta setosa — A root pathogen of lupins

Pleiochaeta setosa — A root pathogen of lupins (iii) A PSTV testing program will be established and a of locations throughout the wheatbeit, being isolated sample of potato tubers from P.R.S. will be tested from 83% of diseased root pieces cultured on WA + A. for PSTV infection each season and continued for Pathogenicity tests were carried out using (1) about 5 years to ensure that the station is free of colonised white millet seed, and (2) conidia, as PSTV. inoculum. Inoculum was uniformiy mixed with pasteurised (70°C for 40 min.) medium-coarse sand in A~knowledgement. 400 ml pots which were kept in the growth room for two "he authors wish to thank Dr. R.H. Symons for weeks prior to sowing. Millet seed inoculum was added conducting the eDNA tests for PSTV and Mrs. Tatyana at 0.3% (w/w) and conidia at 500 per gram of sand (dry weight basis). Control pots received 0.3% (w/w) of Viti for technical assistance. uncolonised millet seed or no conidia respectively. Five Funds for this survey were provided by the seeds (cv. IIlyarrie) were sown per pot. There were ten Commonwealth Department of Health. replicate pots of each treatment. The growth room had a 12 hour photoperiod and a dlurnai temperature Ref.rencee oC http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Australasian Plant Pathology Springer Journals

Pleiochaeta setosa — A root pathogen of lupins

Australasian Plant Pathology , Volume 13 (2) – Jan 27, 2011

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References (6)

Publisher
Springer Journals
Copyright
Copyright
Subject
Life Sciences; Plant Pathology; Plant Sciences; Agriculture; Entomology; Ecology
ISSN
0815-3191
eISSN
1448-6032
DOI
10.1071/APP9840021
Publisher site
See Article on Publisher Site

Abstract

(iii) A PSTV testing program will be established and a of locations throughout the wheatbeit, being isolated sample of potato tubers from P.R.S. will be tested from 83% of diseased root pieces cultured on WA + A. for PSTV infection each season and continued for Pathogenicity tests were carried out using (1) about 5 years to ensure that the station is free of colonised white millet seed, and (2) conidia, as PSTV. inoculum. Inoculum was uniformiy mixed with pasteurised (70°C for 40 min.) medium-coarse sand in A~knowledgement. 400 ml pots which were kept in the growth room for two "he authors wish to thank Dr. R.H. Symons for weeks prior to sowing. Millet seed inoculum was added conducting the eDNA tests for PSTV and Mrs. Tatyana at 0.3% (w/w) and conidia at 500 per gram of sand (dry weight basis). Control pots received 0.3% (w/w) of Viti for technical assistance. uncolonised millet seed or no conidia respectively. Five Funds for this survey were provided by the seeds (cv. IIlyarrie) were sown per pot. There were ten Commonwealth Department of Health. replicate pots of each treatment. The growth room had a 12 hour photoperiod and a dlurnai temperature Ref.rencee oC

Journal

Australasian Plant PathologySpringer Journals

Published: Jan 27, 2011

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