Ravjit K. Khangura
Commonwealth Scientific and Industrial Research Organisation
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Featured researches published by Ravjit K. Khangura.
Phytopathology | 2003
Moin U. Salam; Ravjit K. Khangura; A.J. Diggle; Martin J. Barbetti
ABSTRACT A simple model has been developed to predict the onset of pseudothecia maturity and seasonal ascospore showers in relation to blackleg disease in canola, caused by the fungus Leptosphaeria maculans. The model considers a combination of two weather factors, daily mean temperature and daily total rainfall, to drive progress of maturity of pseudothecia on the infested canola stubble left from past crops. Each day is categorized as suitable or not suitable for progress of the maturation process. The onset of pseudothecia maturity occurs when approximately 43 suitable days have occurred. Following the onset of maturity, ascospore showers are triggered when daily rainfall exceeds a threshold. The model satisfactorily predicted the timing of the onset of pseudothecia maturity when tested with 3 years of field observations at four locations in Western Australia, which characteristically has a Mediterranean climate. The model also agreed reasonably well with the daily pattern of ascospore release observed in two locations. Sensitivity analysis was performed to show the relative importance of the parameters that describe the onset of pseudothecia maturity.
Plant Disease | 1999
Ravjit K. Khangura; Martin J. Barbetti; Mark Sweetingham
A total of 112 Rhizoctonia isolates were collected from various canola (Brassica napus) growing areas of Western Australia. Pectic enzyme electrophoresis differentiated these isolates into six distinct zymogram groups: R. solani, 54% ZG5 (AG2-1), 8% ZG6 (AG2-1), and 1% ZG9 (AG10); binucleate Rhizoctonia, 12% CZG1 (CAG1), 4% CZG4, and 6% CZG5 (AGK); and the remainder unidentified binucleate groups (15%). Binucleate groups were also confirmed by fluorescent nuclear staining and hyphal morphology. One or more isolates from each of the above zymogram groups (including four unidentified binucleate groups) and an isolate of ZG1-1 (AG8) that causes bare patch in cereals and legumes were tested for their pathogenicity on canola. Isolates of ZG5 and ZG1-1 were highly pathogenic on canola, delayed seedling emergence, and caused severe hypocotyl and root rot, respectively. ZG5 also induced postemergence damping-off. Increasing the depth of sowing from 1 to 3 cm significantly delayed seedling emergence and increased disease severity. Four unidentified binucleate isolates (WAC9316, WAC9297, WAC9307, and WAC9290) were moderately pathogenic to canola, while two isolates (WAC9307 and WAC9316) caused significant preemergence damping-off. Two CZG5 isolates were weakly pathogenic. Isolates of ZG5 and ZG1-1 were also tested for their pathogenicity on other rotational crops (narrow-leafed lupin, subterranean clover, wheat, oats, barley, and mustard) and two weed species (wild radish and annual ryegrass). ZG5 caused a severe hypocotyl rot on mustard and mild symptoms of hypocotyl rot on narrow-leafed lupin and clover, but failed to infect any of the cereal hosts, such as wheat, oats, barley, and ryegrass. In contrast, all crops tested were highly susceptible to ZG1-1 except mustard, which was only moderately susceptible. Results indicate that ZG5 is most pathogenic to crucifers and is a mildly virulent pathogen of the leguminous crops but not of cereal crops tested. ZG1-1, known to cause bare patch in legumes and cereals, also can cause severe root rot in canola. This is the first report of hypocotyl rot and pathogenicity of ZG5 on canola in Australia.
Australian Journal of Experimental Agriculture | 2002
S. J. Marcroft; N. Wratten; Agus Purwantara; P. A. Salisbury; Trent Potter; Martin J. Barbetti; Ravjit K. Khangura; Barbara J. Howlett
A range of Brassica species was screened for resistance to Leptosphaeria maculans, the causal agent of blackleg. The lines were assessed in 8 disease nurseries in 4 canola growing regions of Australia and in 1 glasshouse trial, with a view to identifying alternative sources of resistance to L. maculans for Australian breeding programs. Lines were screened for degree of internal and external blackleg symptoms during both the seedling and adult plant growth stages. Correlation for resistance with ranking between disease nurseries was very strong (0.41-0.98). Brassica carinata and B. nigra were the most resistant species in the disease nurseries, being even more resistant than B. juncea. The 7 European winter B. napus lines tested were significantly more resistant than the 7 Australian spring B. napus lines, with another crucifer, Sinapis alba, being intermediate in resistance between the European and Australian B. napus lines. The same ranking of lines from most to least resistant was also seen when cotyledons and stems were inoculated in the glasshouse with 2 well-characterised Australian isolates. With the exception of the B. napus susceptible control Westar, all lines had similar frequencies of seedling survival in the nurseries. However, mature plants of these lines varied significantly in their degree of resistance. This indicates that screening for seedling survival is not useful in selecting L. maculans resistant lines in Australia. The Brassica lines with the B genome, especially B. carinata, and the winter B. napus types are now being used as sources of resistance in Australian breeding programs.
Phytopathology | 2007
Ravjit K. Khangura; J. Speijers; Martin J. Barbetti; Moin U. Salam; A.J. Diggle
ABSTRACT The timing of maturation of pseudothecia and discharge of ascospores of the blackleg fungus (Leptosphaeria maculans) is critical in relation to infection early in the cropping season of canola. During 1998 to 2000, development of pseudothecia was investigated on residues of the previous years canola crop collected from four agroclimatically different locations: Mount Barker (southern high rainfall), Wongan Hills (central medium rainfall), Merredin (central low rainfall), and East Chapman (northern low rainfall) in Western Australia. The pseudothecia matured on residues at different times after harvest in various regions. In general, pseudothecia maturity occurred earlier in the high-rainfall areas than in medium- and low-rainfall areas. An ascospore discharge pattern was investigated from residues of crop from the previous year (6-month-old residues) at three locations-Mount Barker, Wongan Hills, and East Chapman in Western Australia-and from 18-month-old residues that were burnt and raked in the previous year at Mount Barker and East Chapman. Ascospore discharge commenced earlier in high-rainfall (>450 mm) areas (Mount Barker) and late in northern low-rainfall (<325 mm) areas (East Chapman). The major ascospore showers took place during May (late autumn) and June (early winter) at Mount Barker and during July and August (mid- to late winter) at East Chapman. The number of ascospores discharged was extremely low at East Chapman compared with Mount Barker. At both locations, the number of ascospores discharged from 18-month-old residues that were raked and burnt in the previous year were only approximately 10% of those discharged from previous years residues left undisturbed. The discharge of ascospores on any given day was negatively correlated with accumulated temperatures, maximum temperature, evaporation, minimum and maximum soil temperatures, and solar radiation and was positively correlated with the minimum temperature, rain, and minimum relative humidity. This is the first report describing how pseudothecia mature on residues in different rainfall areas in Western Australia, and it potentially can be used in developing a forecasting system to avoid the synchronization of major ascospore showers with the maximum susceptibility period of canola seedlings.
Crop & Pasture Science | 2002
Ravjit K. Khangura; Martin J. Barbetti
The efficacy of the fungicide Impact® (a.i. flutriafol at 250 g/L) was tested for control of blackleg (Leptosphaeria maculans), and for improved yield and oil content in canola (Brassica napus) cultivars with varying levels of blackleg resistance. Field trials were conducted in 1996 in Western Australia at 3 locations (Merredin, Wongan Hills, Mt Barker) in paddocks containing 1–4-year-old blackleg-infested residues. The fungicide (400 mL product/ha) was coated on a double superphosphate fertiliser and applied at seeding. Blackleg was substantially reduced and the seed yield improved following the application of Impact® in most treatments at all locations except Mt Barker, where the fungicide had no effect on reducing the blackleg severity. The percentage reduction in blackleg severity with Impact® ranged between 18 and 59% and 1 and 43% at Merredin and Wongan Hills, respectively, in cultivars with different levels of resistance and exposed to infected residues of various ages. Likewise, the application of Impact® increased the seed yield by 40–322, 186–357, and 71–426 kg/ha at Merredin, Wongan Hills, and Mt Barker, respectively, on residue of various ages. Seed oil content was also improved following the application of Impact® in most treatments at all locations. The improvement in seed yield when using Impact® was variable for different ages of the residue, and was greater under severe to moderate disease conditions caused by exposure to more recent residues than under the milder disease conditions resulting from older residues. In general, susceptible to moderately resistant cultivars showed greater improvement in yield than resistant cultivars. The rates of Impact® were further evaluated in paddocks containing 3-year-old residue in field trials at the same 3 locations during 1997. The fungicide was applied at 200, 400, and 800 mL product/ha. Although blackleg severity was substantially reduced following application of Impact® at 400 and 800 mL/ha compared with 0 and 200 mL/ha, yield was improved only in some cultivars and at some locations.
Australasian Plant Pathology | 2016
A. P. Van de Wouw; Alexander Idnurm; J. A. Davidson; S. J. Sprague; Ravjit K. Khangura; Andrew Ware; Kurt Lindbeck; S. J. Marcroft
Fungal diseases are the major constraint on canola (Brassica napus) production in Australia and worldwide. Blackleg (caused by Leptosphaeria maculans) and Sclerotinia stem rot (Sclerotinia sclerotiorum) are the predominant diseases limiting production but, with increased intensification of production, other diseases previously considered of minor importance and sporadic may be increasing in prevalence. We report on the incidence and severity of four ‘minor’ diseases of canola in Australia: white leaf spot (caused by Pseudocercosporella capsellae), downy mildew (Peronospora parasitica), Alternaria leaf and pod spot (Alternaria brassicae) and powdery mildew (Erysiphe cruciferarum). Diseases were monitored at more than 30 sites across Australia from 2013 to 2015. Regions were identified in which specific diseases are a consistent problem, such as white leaf spot in Hamilton in Victoria. In these regions, control strategies to minimise disease may be required. Varietal differences were observed for some diseases suggesting that resistance to these pathogens is already present in Australian advanced breeding material. Lastly, fungicide applications were shown to control some diseases such as white leaf spot.
Crop & Pasture Science | 2018
S. J. Sprague; Stephen J. Marcroft; Kurt Lindbeck; Andrew Ware; Ravjit K. Khangura; Angela P. Van de Wouw
Abstract. Blackleg, caused by Leptosphaeria maculans, is the main disease constraint for canola production in Australia. The fungus infects all aboveground and belowground parts of the canola plant. Yield loss in Australia and worldwide is generally associated with cankers at the crown, which arise from leaf infections during the early stages of seedling growth. Infection of flowers, peduncles, siliques, main stems and branches, with resultant lesions and canker formation, are typically uncommon symptoms. We propose the term ‘upper canopy infection’ to encompass symptoms on all of these plant parts because they generally occur together on the same plant and appear after the plant has undergone elongation. Branch and stem lesions observed in a commercial crop in 2010 were confirmed as L. maculans. Since then, assessment of upper canopy symptoms at 25 sites across the canola-producing regions of Australia between 2011 and 2016 show that symptoms are more prevalent, although they differed between sites and seasons. In 2011, symptoms were present at a single site, and this increased to seven sites in 2013 and 23 sites in 2016. Preliminary data indicate that infection arises from both ascospore and pycnidiospore inoculum, and that earlier onset of flowering is a key risk factor for more severe upper canopy infection. Evidence suggests that host genetic resistance may be an effective control for upper canopy infection.
Field Crops Research | 2014
Angela P. Van de Wouw; Stephen J. Marcroft; Andrew Ware; Kurt Lindbeck; Ravjit K. Khangura; Barbara J. Howlett
Australasian Plant Pathology | 2015
Vicki L. Elliott; Robert M. Norton; Ravjit K. Khangura; P. A. Salisbury; S. J. Marcroft
Agriculture Western Australia. Farmnote | 2004
Ravjit K. Khangura; G. Walton; Martin J. Barbetti
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