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Figure 8: (A) Photomicrograph of tichomes of Azolla with those of Anabaena surrounding them. (B) Tichomes of Anabaena from
Azolla . Photograph courtesy E. S. Pierson 1 , L. Masselink 2 and M. M. L. van Kempen 2 , Departments of General Instruments 1 and
Aquatic Ecology & Environmental Biology 2 , Faculty of Science, Mathematics and Computing Science, Radboud University,
Huygensgebouw, Heyendaalseweg 135, NL-6525, AJ Nijmegen, The Netherlands.
Differences in morphological and physiological characteristics between cultures of Azolla
symbionts and the fresh isolates from Azolla plants have been studied by the application of
immunological and lectin hemagglutination studies (Newton and Herman, 1979; Gates, 1980;
Ladha and Watanabe, 1982; McCowen et al ., 1987). The role of lectins in establishing Azolla - Anabaena
symbiosis has been examined (Mellor et al ., 1981). Agglutination of human erythrocytes was caused
by extracts from A. caroliniana - Anabaena symbiosis and Anabaena -free Azolla plants whereas extracts
of fresh symbionts from A . caroliniana or A . azollae cultures did not cause agglutination of human
erythrocytes. Kobiler et al . (1981) observed haemagglutination activity in extracts of free-living
A . azollae and very low activity in those from A . fi liculoides - Anabaena symbiosis. Ladha and Watanabe
(1982) reported that there exists a high antigenic similarity between Anabaena freshly isolated from
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