Zoospore induction, morphology, and movement were compared in nine cultures of Fritschiella tuberosa Iyengar collected worldwide. Submerging this terrestrial alga in soil water medium induced zoospore release during the following light period. Zoospores were produced one per cell in all photosynthetic parts of the thallus. Zoospores were anteriorly quadriflagellate and, although lacking eyespots, they exhibited positive phototaxis. Zoospores varied from 4.4 to 13.1 /'m in diameter. Within each culture the sizes formed a normal distribution. All nine cultures had been designated as Fritschiella tuberosa by their respective isolators. The uniformity found in zoospore behavior and morphology supported these identifications. Fritschiella tuberosa Iyengar has been reported from several locations around the world (Table 1). Samples from all these localities were obtained and grown under controlled conditions as a means of comparing these cultures. Since the discovery of this green alga in 1932, F. tuberosa has stirred great interest evolutionarily due to its advanced morphology and its growth in a terrestrial habitat (Fott 1965, Fritsch 1945, Pickett-Heaps 1975, Scagel et al. 1965). The thallus is differentiated into distinct parenchymatous prostrate and filamentous upright photosynthetic portions as well as nonphotosynthetic rhizoidal filaments (Iyengar 1932). When conditions are favorable, especially during periods of flooding, F. tuberosa has the ability to reproduce quickly and with great numbers of propagules, which have been shown to be asexual zoospores (Hopkins 1977). This characteristic and the compact nature of the prostrate thallus, which reduces desiccation, are important aspects of the success of this alga in invading the terrestrial habitat. This study analyzed the production of zoospores, their morphology, and their subsequent activity. A comparison of these aspects among the nine geographically diverse collections was undertaken as one means of assessing the monospecificity of these collections, all identified as Fritschiella tuberosa, and as a means of learning more about asexual reproduction in this alga. MATERIALS AND METHODS. The source of each F. tuberosa culture is listed in Table 1. The unialgal clones were maintained in 30 ml capped culture tubes on 1.5% Difco algal agar supplemented with soil water in a 12:12 L:D regime, with
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