Association of Pythium coloratum and Pythium sulcatum with cavity spot disease of carrots in Western Australia

1996 ◽  
Vol 45 (4) ◽  
pp. 727-735 ◽  
Author(s):  
K. A. EL‐TARABILY ◽  
G. E. ST. J. HARDY ◽  
K. SIVASITHAMPARAM
1996 ◽  
Vol 183 (2) ◽  
pp. 279-290 ◽  
Author(s):  
Khaled A. El-Tarabily ◽  
Giles E. St. J. Hardy ◽  
Krishnapillai Sivasithamparam ◽  
Ipek D. Kurtb�ke

1997 ◽  
Vol 45 (4) ◽  
pp. 727 ◽  
Author(s):  
A. El-Tarabily ◽  
Giles E. St J. Hardy ◽  
Krishnapillai Sivasithamparam

Three experiments were conducted with Pythium coloratum Vaartaja, a causal agent of cavity spot disease of carrots in Western Australia, to study the relationships between host age, time of infection and development of cavity spot lesions. Pythium coloratum was isolated frequently from 3-6-week-old asymptomatic roots of carrots grown in soils infested naturally or artificially with the pathogen. Carrots grown in containers of soil artificially infested with P. coloratum, but not those in naturally infested field soil, developed cavity spot lesions after 6 weeks. Early infection of carrot seedlings at or before 3 weeks by P. coloratum in artificially infested soils followed by their transfer to pathogen-free soil was sufficient to cause cavity spot disease at the time of harvest (16 weeks). The disease levels in this treatment were not different from those transferred to P. coloratum-infested soil. There was no significant (P > 0.05) association between carrot age and the ability of P. coloratum to infect the roots and to cause cavity spot lesions at harvest.


1997 ◽  
Vol 37 (2) ◽  
pp. 265 ◽  
Author(s):  
K. A. El-Tarabily ◽  
G. E. St J. Hardy ◽  
K. Sivasithamparam ◽  
A. G. McKay

Summary. Glasshouse trials were conducted to examine the effect of lime or gypsum amendments on the development of cavity spot disease of carrots in soil artificially infested with Pythium coloratum. Each amendment was applied to soil from the field at 4000 or 8000 kg/ha. Lime at both application rates significantly (P<0.05) reduced the incidence of the disease. In contrast, both gypsum treatments had no effect on the incidence of cavity spot disease. There was no significant (P>0.05) difference in calcium concentration between carrot roots grown in unamended, lime- or gypsum-amended soil with or without the pathogen. Calcium did not appear to play a direct role in the reduction of cavity spot disease. Under the controlled conditions of this glasshouse trial, reduction in the incidence of cavity spot appeared to be related to the increase in soil pH associated with the application of lime. Field trials at the site of soil collection will confirm whether this mechanism is related to field reduction of the disease following liming.


1997 ◽  
Vol 137 (3) ◽  
pp. 495-507 ◽  
Author(s):  
KHALED A. EL-TARABILY ◽  
GILES E. ST. J. HARDY ◽  
KRISHNAPILLAI SIVASITHAMPARAM ◽  
ASSEM M. HUSSEIN ◽  
D. IPEK KURTBOKE

Plant Disease ◽  
2014 ◽  
Vol 98 (6) ◽  
pp. 790-796 ◽  
Author(s):  
Hieu Sy Tran ◽  
Yu Pin Li ◽  
Ming Pei You ◽  
Tanveer N. Khan ◽  
Ian Pritchard ◽  
...  

Black spot (also referred to as Ascochyta blight, Ascochyta foot rot and black stem, and Ascochyta leaf and pod spot) is a devastating disease of pea (Pisum sativum) caused by one or more pathogenic fungi, including Didymella pinodes, Ascochyta pisi, and Phoma pinodella. Surveys were conducted across pea-growing regions of Western Australia in 1984, 1987, 1989, 1996, 2010, and 2012. In total, 1,872 fungal isolates were collected in association with pea black spot disease symptoms. Internal transcribed spacer regions from representative isolates, chosen based on morphology, were sequenced to aid in identification. In most years and locations, D. pinodes was the predominant pathogen in the black spot complex. From 1984 to 2012, four new pathogens associated with black spot symptoms on leaves or stems (P. koolunga, P. herbarum, Boeremia exigua var. exigua, and P. glomerata) were confirmed. This study is the first to confirm P. koolunga in association with pea black spot symptoms in field pea in Western Australia and show that, by 2012, it was widely present in new regions. In 2012, P. koolunga was more prevalent than D. pinodes in Northam and P. pinodella in Esperance. P. herbarum and B. exigua var. exigua were only recorded in 2010. Although A. pisi was reported in Western Australia in 1912 and again in 1968 and is commonly associated with pea black spot in other states of Australia and elsewhere, it was not recorded in Western Australia from 1984 to 2012. It is clear that the pathogen population associated with the pea black spot complex in Western Australia has been dynamic across time and geographic location. This poses a particular challenge to development of effective resistance against the black spot complex, because breeding programs are focused almost exclusively on resistance to D. pinodes, largely ignoring other major pathogens in the disease complex. Furthermore, development and deployment of effective host resistance or fungicides against just one or two of the pathogens in the disease complex could radically shift the make-up of the population toward pathogen species that are least challenged by the host resistance or fungicides, creating an evolving black spot complex that remains ahead of breeding and other management efforts.


2014 ◽  
Vol 140 (3) ◽  
pp. 597-605 ◽  
Author(s):  
Hieu Sy Tran ◽  
Ming Pei You ◽  
Tanveer N. Khan ◽  
Ian Pritchard ◽  
Martin J. Barbetti

1998 ◽  
Vol 27 (3) ◽  
pp. 163 ◽  
Author(s):  
E.M. Davison ◽  
A.G. McKay

2010 ◽  
Vol 58 (5) ◽  
pp. 392
Author(s):  
E. M. Davison ◽  
F. C. S. Tay

Hakea myrtoides Meisn. is an attractive shrub that has a restricted distribution in the south-west of Western Australia. It is not killed by fire but re-sprouts from basal lignotubers. Its leaves are often severely affected by tar spot disease, caused by the biotrophic, stromatic ascomycete Phyllachora grevilleae (Lév.) Sacc. subsp. grevilleae (Lév) Sacc. This disease is spread by ascospores that are produced during the wettest months of the year: late autumn, winter and spring. Badly infected populations of H. myrtoides were burnt, either in a controlled burn in November 2007, or in a wildfire in January 2008. The incidence of tar spot disease on leaves of burnt plants in 2008 and 2009 was 4.4%, while its incidence on unburnt plants was significantly higher (25.1%). The incidence of flowering in 2009 was similar in both burnt and unburnt populations. Tar spot disease is common on H. myrtoides; it is present on 77% of collections of this host in the Western Australian Herbarium (PERTH).


Author(s):  
M. A. Spencer

Abstract A description is provided for Pythium coloratum. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. DISEASES: Carrot cavity-spot, seedling damping-off. HOSTS: Apium graveolens, Daucus carota (Apiaceae); Zantedeschia aethiopica (Araceae); Lactuca sativa (Asteraceae); Brassica oleracea (Brassicaeae); Beta vulgaris (Chenopodiaceae); Cucumis sativus (Cucurbitaceae); Persea americana (Lauraceae); Allium cepa (Liliaceae s.l.); Pinus radiata (Pinaceae); Lycopersicon esculentum (Solanaceae). GEOGRAPHICAL DISTRIBUTION: NORTH AMERICA: Canada (British Columbia, Ontario), USA (New York). ASIA: Iran, Taiwan. AUSTRALASIA: Australia (South Australia, Western Australia), New Zealand. EUROPE: Great Britain. TRANSMISSION: Contaminated soil, organic matter (oospores) and water (sporangia).


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