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Phytophthora alni complex (P. × alni, P. × multiformis, P. uniformis) are pathogens attacking alder seedlings and trees, causing significant losses in nurseries and natural tree stands. Decay of alder trees has been observed in Poland for over a dozen years. Overall, 25 Polish isolates of P. × alni obtained from symptomatic alder trunks, rhizosphere soil surrounding infected trees, and nearby natural streams were compared with isolates from symptomatic trunks obtained in France, Belgium and Hungary. Morphologic characterization of mycelium, vegetative and generative organs, temperature effect on mycelium growth, and their pathogenicity were studied. The mycelium growth rate of isolates from symptomatic plants was fastest on Carrot Agar (CA) medium, and from soil and water on Vegetable Agar (V8A) medium. The sizes of zoosporangia varied depending on their origin. The isolates that originated from the soil had the largest zoosporangia. The diameter of the oogonia and antheridia did not differ regardless of their origin. The results of pathogenicity tests of P. × alni isolates obtained from different sources showed that the soil isolates were the most aggressive in each test, followed by the isolates from the trunks and water. A simple test of leaf colonization can give an idea of the aggressiveness of the isolate towards the shoots and roots. No morphological or physiological markers of aggressiveness have been found.

Phytophthora alni complex (P. × alni, P. × multiformis, P. uniformis) are pathogens attacking alder seedlings and trees, causing significant losses in nurseries and natural tree stands. Decay of alder trees has been observed in Poland for over a dozen years. Overall, 25 Polish isolates of P. × alni obtained from symptomatic alder trunks, rhizosphere soil surrounding infected trees, and nearby natural streams were compared with isolates from symptomatic trunks obtained in France, Belgium and Hungary. Morphologic characterization of mycelium, vegetative and generative organs, temperature effect on mycelium growth, and their pathogenicity were studied. The mycelium growth rate of isolates from symptomatic plants was fastest on Carrot Agar (CA) medium, and from soil and water on Vegetable Agar (V8A) medium. The sizes of zoosporangia varied depending on their origin. The isolates that originated from the soil had the largest zoosporangia. The diameter of the oogonia and antheridia did not differ regardless of their origin. The results of pathogenicity tests of P. × alni isolates obtained from different sources showed that the soil isolates were the most aggressive in each test, followed by the isolates from the trunks and water. A simple test of leaf colonization can give an idea of the aggressiveness of the isolate towards the shoots and roots. No morphological or physiological markers of aggressiveness have been found. [ABSTRACT FROM AUTHOR]