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First report of crater rot caused by Rhizoctonia
carotae on carrots (Daucus carota L.) in Turkey
S. Kurt*, E.M. Soylu, S. Soylu and F.M. Tok
Department of Plant Protection, Faculty of Agriculture, University of
Mustafa Kemal, 31040 Hatay, Turkey
*senerk31040@yahoo.com
Accepted for publication 15/11/04
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Figure 1: Typical crater rot caused by R. caratoe on
carrot roots. Note dark brown decay (arrows) around the crown and
upper parts of the root.
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Crater rot was observed on carrots
growing in fields in the eastern Mediterranean region of Turkey; one
of the country’s main production areas. Relatively high humidity
and cool conditions of the 2002 and 2003 growing seasons may have
been factors that influenced the severe disease incidences that were
observed (47.6 and 53.2% respectively). This resulted in 55 to 70%
yield reductions in the fields inspected.
Primary symptoms seen were a band of dark brown necrosis around
the carrot crown and horizontal brown canker-like lesions mostly on
the crown and upper roots (Fig. 1). Small pits subsequently
developed beneath the lesions, that enlarged into sunken brown
crater lines with a white, flocculent mycelium produced under high
humidity. Sections cut from infected carrot roots were
surface-sterilised in 1% NaOCl for 2 min, plated on 2.0% water agar
medium supplemented with 50 mg/L streptomycin sulphate, and
incubated for 7 to 10 days at 24 ± 2°C. Hyphal tips from the
margin of each developing Rhizoctonia colony were subcultured
on potato dextrose agar (PDA). Fungal colonies were initially white
and turned brown with age. Dark brown to black sclerotia were
occasionally produced (Fig. 2A). Hyphae occasionally had long,
multinucleate swollen cells. Hyphal branches arose at right angles
and contained a cross-wall near the branch point. Clamp connections
were observed in the hyphae (Fig. 2B). The causal organism was
identified as Rhizoctonia carotae based on these
morphological characteristics (Rader, 1948; Jensen, 1971). |
Koch’s postulates were completed by inoculating wounded carrot
roots with 5mm-PDA plugs, bearing both mycelium and sclerotia of the
isolated pathogen. Inoculated carrots were kept in a moist chamber (100%
RH) at 23°C for 14 days. Control carrots were sterilised with 2% NaOCl
and treated with uninoculated PDA plugs in a similar manner. Small
brownish sunken lesions, identical to those observed in
naturally-infected carrots, became visible 5-7 days after inoculation.
No lesions were observed on control carrots. The pathogen was
successfully re-isolated from inoculated carrots, thereby completing
Koch’ s postulates.
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Figure 2: A Typical dark brown sclerotia (*) and swollen
hyphae (arrow) of the pathogen. B Hyphal clamp connection
(arrow). |
R. carotae has previously been reported from USA (Rader, 1948;
Punja, 1987), Denmark, Norway, Sweden, Russia (Jensen, 1971) and the UK
(Derbyshire & Crisp, 1978). This is the first report of R.
carotae on carrots in Turkey.
References
Derbyshire DM, Crisp AF, 1978. Studies on treatments to prolong the
storage life of carrots. Experimental Horticulture 30,
23-28.
Jensen A, 1971. Storage diseases of carrots, especially Rhizoctonia
crater rot. Acta Horticulturae 20, 125-129.
Punja ZK, 1987. Mycelial growth and pathogenesis by Rhizoctonia
carotae on carrot. Canadian Journal of Plant Pathology 9,
24-31.
Rader WE, 1948. Rhizoctonia carotae n. sp. and Gliocladium
aureum n. sp., two new root pathogens of carrots in cold storage. Phytopathology
38, 440-452.
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