Asterionella formosa

Asterionella formosa is the type species of its genus, Asterionella.[1]

Asterionella formosa ranges from 45–68 micrometres (0.0018–0.0027 in) in length and 1.1–4.5 µm in width. Asterionella formosa has valves (siliceous plate that makes up a half of a diatom cell) that are long and narrow, with capitate (enlarged and rounded) apices (tips) unequal in size. The larger apex is known as the footpole. A. formosa has a very narrow sternum (thickened, longitudinal section of the silica valve) and irregularly spaced striae (rows of pores on the valve surface), slightly offset from one another at the sternum. Some A. formosa have irregularly spaced marginal spines between striae. At each end, there is a porefield (area of pores with a different pattern). Rimoportulas (round apertures) have been observed to occur at either or both ends of the valve.[3]

Within each cell is a nucleus at their center and 6–8 golden-brown chromatophores.[4]

Asterionella formosa colonies consist of cells joined at their valve faces' footpoles by mucilage pads.[3] Their colonies consist of 8–20 cells and take on a spiral, star-like shape. They may also occur in a closed ring shape, but this is rare.[4]

Asterionella formosa is common in mesotrophic and eutrophic lakes and slow-moving river plankton around the world, and is especially common in the northern hemisphere. It has become increasingly common in oligotrophic (low-nutrient) mountainous lakes.[3]

Asterionella formosa colonies may be colonized by small, sessile (non-mobile) choanoflagellates, or infested by Zygorhizidium planktonicum, a parasitic chytrid fungus. To prevent the fungus from spreading, affected cells in the colony usually induce cell death.[4]

A. formosa laboratory models have been observed to have dynamic microbiomes with many bacterial species, mostly from the phylums Proteobacteria and Bacteroidetes. Most of the bacteria were heterotrophic and more than half could metabolize glycolate.[5]