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Reproductive biology of Stictosiphonia hookeri (Rhodomelaceae, Rhodophyta) from Argentina, Chile, South Africa and Australia in laboratory culture

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Karsten,  Ulf
Permanent Research Group Microsensor, Max Planck Institute for Marine Microbiology, Max Planck Society;

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Citation

West, J., Zuccarello, G., & Karsten, U. (1996). Reproductive biology of Stictosiphonia hookeri (Rhodomelaceae, Rhodophyta) from Argentina, Chile, South Africa and Australia in laboratory culture. Hydrobiologia, 327, 277-282.


Cite as: https://hdl.handle.net/21.11116/0000-0004-F8D5-4
Abstract
The red alga Stictosiphonia hookeri is epilithic in shaded habitats of the upper intertidal zone from 30 to 55 degrees S. Thalli of this species from Argentina, Chile, South Africa and Australia, usually without reproductive structures when collected, all developed tetrasporangia in culture. Although good vegetative growth occurred in all nine isolates at 20-25 degrees C, 12:12 light: dark cycle, 10-30 mu mol photons m(-2) s(-1), none reproduced in these conditions except one isolate from Australia. At 15 degrees C the four South African (34 degrees S) isolates developed tetrasporangial stichidia, and three completed a Polysiphonia-type life history. Gametophytes were unisexual or bisexual. At 15 degrees C one isolate from Chile (36 degrees S) formed tetrasporangia, but sporelings were not viable. At 10 degrees C isolates from Argentina and Chile (53 degrees S and 54 degrees S) formed tetrasporangia; however, only the Chile isolate completed a Polysiphonia-type life history with unisexual gametophytes. The temperature required to induce sporogenesis correlates with the range of water and air temperatures in the natural habitats of each isolate. In irradiances >50 mu mol m(-2) s(-1) the thalli became yellow- brown within two weeks because of phycobiliprotein loss, but this did not impair growth or reproduction. The Argentina and Chile isolates were resistant to freezing in seawater for at least two days, showing no cell damage. The protein cuticle of the outer cell wall is repeatedly shed in culture. This may serve to minimize the attachment of epiphytes in the field.