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Annual Report 2006

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using dormant winter buds. Also, we started<br />

three cryopreservation projects such as<br />

practical storage of -grown potato<br />

shoots, development of cryopreservation protocol<br />

of mat rush and sugarcane. In these, practical<br />

cryopreservation method of -grown<br />

potato shoot tips by encapsulation-vitrification<br />

was improved. Mass propagation system of <br />

-grown mat rush shoots was established<br />

using induction of multiple shoots.<br />

Morphological, molecular and<br />

phytopathological variations of<br />

<br />

(van Beyma) M.E.<br />

Palm, W. Gams & Nirenberg, which was validly<br />

described in 1995 (Palm et al. 1995), had been<br />

known as a common soil fungus at rhizospheres,<br />

and was isolated from lake sediment for the<br />

first time in Japan (Tubaki and Ito, 1975). We<br />

identified several fungal isolates pathogenic to<br />

plants, pumpkin, garden ranunculus, anemone,<br />

sweet pepper, lotus ginger and Japanese radish<br />

(Fig. 3), as and found that it had<br />

been differentiated morphologically, molecularly<br />

and phytopathologically. The isolates used are<br />

shown in Table 1. Their morphological<br />

characters are as follows (Fig. 4). Colonies in<br />

culture on potato dextrose agar (PDA) at 20in<br />

the dark are flat with little aerial mycelium,<br />

smooth and cream to salmon or pale brown in<br />

color. Conidiophores are unbranched or<br />

occasionally branched, with conidiogenous cells<br />

often arising at right angles from vegetative<br />

hyphae. Conidiogenous cells are monophialides<br />

or rarely polyphialides formed at the apices, or<br />

as short (adelophialides) or long blanches from<br />

vegetative hyphae, hyaline, smooth, cylindrical<br />

to obclavate, sometimes crooked or sinuous at<br />

the tips, often with single conidiogenous<br />

apertures, and occasionally with second<br />

apertures. Conidia are produced in colorless<br />

slime masses at the tips of the phialides, hyaline,<br />

smooth, oblong-ellipsoidal, usually asymmetrical<br />

to slightly curved, multiguttlate and most are 1-<br />

septate and with a few aseptate.<br />

Growth speed of mycelia and appearance<br />

rates of aseptate conidia on PDA at 20in the<br />

dark varied from 2.7-4.7 mm/day and 0-28.6%,<br />

respectively, in 6-8 isolates. Sizes of septate and<br />

aseptate conidia that had formed on synthetic<br />

low nutrient agar (SNA) at 20in the dark<br />

ranged from 4.0-12.01.0-5.5 µm and 2.5-8.51.0-<br />

3.5 µm, respectively, depending on the isolates.<br />

The 10 isolates were classified into 2 groups<br />

based on their sequence data of rDNA ITS<br />

Fig. 3<br />

Diseases of pumpkin (A), garden ranunculus (B),<br />

anemone (C), sweet pepper (D) , lotus ginger (E) and<br />

Japanese radish (F) caused by <br />

Fig. 4<br />

Colonies of on potato dextrose agar<br />

plates (upper left: surface view, upper right: reverse<br />

view), conidiogenous cells and conidia of <br />

(lower left: an isolate from pumpkin, lower right: an<br />

isolate from ranunculus)

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