4.1 Article

The dark art of cultivating glacier ice algae

Journal

BOTANY LETTERS
Volume -, Issue -, Pages -

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/23818107.2023.2248235

Keywords

Glacier ice algae; Greenland ice sheet; arctic; cultivation; climate change; microalgae; oligotrophic conditions

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Cultures of Ancylonema sp. were successfully established and maintained for up to 2 years by optimizing growth media and parameters. The genetic diversity of these cultures was found to be rich, and they were confirmed to belong to the same clade as A. nordenskioldii and A. alaskanum. Despite successful growth and long-term maintenance, laboratory settings can be further improved for optimal growth conditions.
The Ancylonema genus includes the most-documented microalgae on glaciers and ice sheets worldwide. There is significant interest in these microalgae in the context of climate change, considering their role in lowering surface ice albedo and acceleration of ice melt. However, currently, no cultures of the two closely related species A. nordenskioldii or A. alaskanum have been established, restricting our ability to study these globally important species under laboratory conditions. We established and kept cultures of Ancylonema sp. alive for up to 2 years, by testing and optimizing different growth media and parameters. Maximum growth was achieved when using 1:100 diluted media with soil extract and low light intensity (300 & mu;mol m-2s-1). However, as a consequence of incubation in lab conditions, some of the cultures lost their purpurogallin pigmentation and appeared green. Sanger sequencing of the ribulose-1,5 bisphosphate carboxylase/oxygenase large subunit (rbcL) marker gene revealed a large genetic diversity (possibly cryptic) and confirmed the cultures as falling within the same clade as A. nordenskioldii and A. alaskanum. Growth experiments allowed us to estimate a division rate of between 15 & PLUSMN; 5.2 and 21.9 & PLUSMN; 4.8 days. This is up to 4 times slower than current field-based estimates (3.75-5.5 days) and indicates that, despite the successful growth and long-term maintenance of the cultures, laboratory settings can be further improved to achieve optimal growth conditions.

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