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Vol.55 - Izbis

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36 Jelica Balaž i sar.<br />

Tello, M.L., Redondo, C., Sagasta-Mateo, E. (2000): Health status of plane trees (Platanus<br />

spp.) in Spain. Journal of Arboriculture 26(5): 246-254, Sempteber 2000.<br />

Wulf, A., Butin, H. (1987): Krankheiten und Schädlinge der Platane. Nachrichtenblatt des<br />

Deutschen Pflanzenschutzdienstes, 39(10): 145-148, Stuttgart.<br />

(Primljeno: 05.02.2007.)<br />

(Prihvaćeno: 08.08.2007.)<br />

INFLUENCE OF NUTRIENT MEDIUM AND TEMPERATURES ON<br />

THE ANAMORPH DEVELOPMENT IN-VITRO OF THE FUNGUS<br />

APIOGNOMONIA VENETA, THE PLANE TREES PATHOGEN<br />

BALAŽ JELICA, ARSENIJEVIĆ MOMČILO, POPOVIĆ TATJANA<br />

Faculty of Agriculture, Department of Plant Protection, 21000 Novi Sad<br />

E-mail: marsa@neobee.net<br />

Summary<br />

The effect of nutrient media and various temperatures on the Apiognomonia<br />

veneta (Sacc. & Speg.) Höhn. development in-vitro has not been investigated in<br />

more details, according to available literature.<br />

Results of our investigation were shown that only anamorph of the fungus<br />

has been developed in-vitro. The best media for colonies growth were malt agar,<br />

potato dextrose agar and sour synthetic medium. The prune agar was unfavorable<br />

for pathogen development.<br />

From the four isolates investigated (Pl-57, Pl-58, Pl-61 and Pl-62), the<br />

colonies of Pl-57 and Pl-58 were the smaller on malt and onion agar than Pl-61<br />

and Pl-62 one (Table 1).<br />

But onion and malt agar stimulated conidiomata production which don't<br />

appeared on sour synthetic and dry plum agar (Table 2).<br />

The conidia production of weak degree were only on onion, PDA and<br />

malt agar by Pl-61 and Pl-62 isolates exept Pl-62 one which conidia formed most<br />

intensively (Table 2).<br />

As it was shown nutrient media more influenced on colony growth than<br />

conidia production (Tables 1 and 2). That can be probably explane by presence of<br />

convenient substances in tissues of plane trees in-vivo than in artificial media for<br />

pathogen development in-vitro.

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