Establishing the relationship of ascospore loads with blackleg (Leptosphaeria maculans) severity on canola (Brassica napus)
A. D. Wherrett A C , K. Sivasithamparam A and M. J. Barbetti BA School of Earth and Geographical Sciences, The University of Western Australia, Crawley, WA 6009, Australia.
B School of Plant Biology, Faculty of Natural and Agricultural Sciences, The University of Western Australia, Crawley, WA 6009, Australia.
C Corresponding author; email: wherret@cyllene.uwa.edu.au
Australian Journal of Agricultural Research 55(8) 849-854 https://doi.org/10.1071/AR04026
Submitted: 5 February 2004 Accepted: 4 June 2004 Published: 31 August 2004
Abstract
A study was carried out to determine the relationship of blackleg (Leptosphaeria maculans) to ascospore loads from infested canola residue, and also to determine whether effects of chemicals on L. maculans development and ascospore discharge from residues would be reflected in subsequent disease on a freshly sown crop. Residues were dipped in a water-only control or solutions of flutriafol or glufosinate-ammonium and placed in the field prior to early winter rains where they remained through the growing season. Canola (Brassica napus cv. Dunkeld) was seeded adjacent to residues. Early seedling lesion and adult plant crown canker development were monitored. A significant exponential relationship between numbers of ascospores discharged from residues and seedling percentage disease index (SPDI; range 0–100%) and adult plant percentage disease index (APDI; range 0–100%) was evident. In particular, large variations in SPDI and APDI were evident in relation to changes in level of inoculum where less than 25 × 105 ascospores/stem (approx.) were discharged. A reduction in ascospore numbers discharged from 25 × 105 ascospores/stem to 5 × 105 ascospores/stem resulted in a significant reduction of SPDI and APDI. Above this ascospore/stem threshold, responses to inoculum increases were minimal, with relatively little further increase in SPDI or APDI. Our study established, for the first time, a clear response of disease severity to numbers of ascospores discharged. SPDI was lower in plots containing flutriafol- or glufosinate-ammonium-treated residues compared with water-only control plots. Nearly all seedlings remained symptom-free in flutriafol-treated plots compared with only 20% in the water-only control plots. Crown canker measurement on adult plants indicated significantly lower APDI in plots containing flutriafol- or glufosinate-ammonium-treated residues compared with the untreated control plots. SPDI was highly correlated to APDI.
Additional keywords: rapeseed, Phoma lingam, oilseed rape.
Acknowledgments
We thank the Grains Research and Development Corporation for funding this research. Thanks also to Dr Li Hua for helpful discussions and Mr R. Creasy for help with experimental equipment and fieldwork.
Anon.
(2003) Crop variety sowing guide for Western Australia. Bulletin 4592, Department of Agriculture Western Australia, Perth.
Barbetti MJ
(1995) Resistance in annual Medicago species to Phoma medicaginis and Leptosphaerulina trifolii under field conditions. Australian Journal of Experimental Agriculture 35(
), 209–214.
Barbetti MJ, Khangura RK
(1999) Managing blackleg in the disease-prone environment of Western Australia. ‘Proceedings of the 10th International Rapeseed Congress’. Canberra, Australia.. (Ed. N Wratten )
p. 100. (Groupe Consultatif International de Recherche sur le Colza: Paris, France)
Gladders P, Musa TM
(1980) Observations on the epidemiology of Leptosphaeria maculans stem canker in winter oilseed rape. Plant Pathology 29(
), 28–37.
Hammond KE,
Lewis BG, Musa TM
(1985) A systemic pathway in the infection of oilseed rape plants by Leptosphaeria maculans.
Plant Pathology 34(
), 557–565.
Howlett BJ, Ballinger DJ, Barbetti MJ
(1999) Diseases. ‘Canola in Australia: the first thirty years’. (Eds PA Salisbury, TD Potter, G McDonald, AG Green)
pp. 47–52. (Organising Committee of the 10th International Rapeseed Congress, Elect Printing: Canberra, ACT)
Humpherson-Jones FM, Burchill RT
(1982) Chemical suppression of the sexual stage of Leptosphaeria maculans on oil-seed rape and turnip seed crop straw. Annals of Applied Biology 100(
), 281–288.
James WC,
Shih CS,
Callbeck LC, Hodgson WA
(1973) Interplot interference in field experiments with late blight of potato (Phytophthora infestans). Phytopathology 63(
), 1269–1275.
Khangura RK, Barbetti MJ
(1999) Chemical control of blackleg disease of canola in Western Australia. ‘Proceedings of the 10th International Rapeseed Congress’. Canberra, Australia.. (Ed. N Wratten ,
TD Potter ,
G McDonald ,
AG Green )
p. 232. (Groupe Consultatif International de Recherche sur le Colza: Paris)
Khangura RK, Barbetti MJ
(2002) Efficacy of Impact® to manage blackleg (Leptosphaeria maculans) in canola. Australian Journal of Agricultural Research 53(
), 311–321.
| Crossref | GoogleScholarGoogle Scholar |
Li H,
Sivasithamparam K, Barbetti MJ
(2003) Breakdown of a Brassica rapa ssp. sylvestris dominant blackleg resistance gene in B. napus rapeseed by Leptosphaeria maculans field isolates in Australia. Plant Disease 87(
), 752.
Marcroft SJ,
Sprague SJ,
Pymer SJ,
Salisbury PA, Howlett BJ
(2003) Factors affecting the survival and dissemination of the blackleg fungus (Leptosphaeria maculans) in south-eastern Australia. Australian Journal of Experimental Agriculture 43(
), 1231–1236.
| Crossref | GoogleScholarGoogle Scholar |
McArthur, WM (1991).
McGee DC, Emmett RW
(1977) Blackleg (Leptosphaeria maculans (Desm.) Ces.et de Not.) of rapeseed in Victoria: crop losses and factors which affect disease severity. Australian Journal of Agricultural Research 28(
), 47–51.
| Crossref |
McGee DC, Petrie GA
(1979) Seasonal patterns of ascospore discharge by Leptosphaeria maculans in relation to blackleg of oilseed rape. Phytopathology 69(
), 586–589.
McKinney HA
(1923) Influence of soil and moisture on infection of wheat seedlings by Helminthosporum sativum.
Journal of Agricultural Science 26(
), 195–218.
Petrie GA
(1995) Effects of chemicals on ascospore production by Leptosphaeria maculans on blackleg-infected canola stubble in Saskatchewan. Canadian Plant Disease Survey 75(
), 45–50.
Rawlinson CJ,
Muthyalu G, Cayley GR
(1984) Fungicide effects on light leaf spot, canker, crop growth and yield of winter oil-seed rape. Journal of Agricultural Science, Cambridge 103(
), 613–628.
Salam MU,
Khangura RK,
Diggle AJ, Barbetti MJ
(2003) Blackleg sporacle: a model for predicting onset of pseudothecia maturity and seasonal ascospore showers in relation to blackleg of canola. Phytopathology 93(
), 1073–1081.
Salisbury PA,
Ballinger DJ,
Wratten N,
Plummer KM, Howlett BJ
(1995) Blackleg disease on oilseed Brassica in Australia: a review. Australian Journal of Experimental Agriculture 35(
), 665–672.
Turkington TK,
Clayton GW, Woods DL
(2000) The impact of soil incorporation of canola residues and stubble application of chemicals on decomposition and inoculum production by Leptosphaeria maculans.
Canadian Journal of Plant Pathology 22(
), 155–159.
West JS,
Kharbanda PD,
Barbetti MJ, Fitt BDL
(2001) Epidemiology and management of Leptosphaeria maculans (phoma stem canker) on oilseed rape in Australia, Canada and Europe. Plant Pathology 50(
), 10–27.
| Crossref | GoogleScholarGoogle Scholar |
Wherrett AD,
Sivasithamparam K, Barbetti MJ
(2003) Chemical manipulation of Leptosphaeria maculans (blackleg disease) pseudothecial development and timing of ascospore discharge from canola (Brassica napus) residues. Australian Journal of Agricultural Research 54(
), 837–848.
| Crossref | GoogleScholarGoogle Scholar |