Nature 325, 616 - 617 (18 February 1987); doi:10.1038/325616a0

An endogenous annual clock in the toxic marine dinoflagellate Gonyaulax tamarensis

Donald M. Andersen & Brace A. Keafer

Biology Department, Woods Hole Oceanographic Institution, Woods Hole, Massachusetts 02543, USA

Blooms of the toxic dinoflagellate Gonyaulax tamarensis (synonyms Protogonyaulax tamarensis ¹ and Alexandrium tamarense ²) cause outbreaks of paralytic shellfish poisoning (PSP) in coastal waters throughout the world. In the Gulf of Maine, episodes occur between April and November, a seasonally due in part to life-cycle alternations between motile, vegetative cells and resting cysts which overwinter in bottom sediments^3,4. Newly formed cysts have a mandatory 2–6 month dormancy period during which germination is not possible⁵, but once mature, the resting state will continue if temperatures are unfavourable⁵ or oxygen is unavailable⁶. We now report another factor controlling germination of cysts of G. tamarensis from deep coastal waters—an endogenous annual clock that can override an otherwise favourable environment for germination. Similar annual variability in germination has not been observed for cysts of this species from shallow estuaries. These results represent the first conclusive demonstration of an endogenous circannual rhythm in a marine plant. They are evolutioiiarily and ecologically significant because an endogenous annual clock can lead to the release of motile cells into deep and relatively invariant bottom waters at those times when temperature and light at the surface are suitable for growth. In shallow waters where seasonal variability is large and extends to bottom sediments, a strategy similar to that of the seeds of terrestrial plants would be more appropriate, namely a direct coupling between germination and the external environment.

References

1.	Taylor, F. J. R. in Toxic Dinoflagellates (eds Anderson, D. M., White, A. W. & Baden, D. G.) 11−26 (Elsevier, New York, 1985). | ChemPort |
2.	Balech, E. in Toxic Dinoflagellates (eds Anderson, D. M., White, A. W. & Baden, D. G.) 33−38 (Elsevier, New York, 1985).
3.	Dale, B. Sarsia 63, 29−34 (1977).
4.	Anderson, D. M. & Wall, D. J. Phycol. 14, 224−234 (1978). | ISI |
5.	Anderson, D. M. J. Phycol. 16, 166−172 (1980). | Article |
6.	Anderson, D. M., Taylor, C. D. & Armbrust, E. V. Limnol. Oceanogr. (in the press).
7.	Famer, D. S. A. Rev. Physiol. 47, 65−82 (1985).
8.	Kenagy, G. J. Comp. Biochem. Physiol. 134, 333−340 (1981).
9.	Sweeney, B. M. Rhythmic Phenomena in Plants (Academic, New York, 1969).
10.	Karssen, C. M. Israel J. Bot. 29, 45−64 (1981).
11.	Bewley, J. D. & Black, M. Physiology and Biochemistry of Seeds in Relation to Germination Vol. 2 (Springer, Berlin, 1982).
12.	Yentsch, C. M. & Mague, F. C. Int. J. Chronobiol 7, 77−84 (1980).
13.	Dale, B., Yentsch, C. M. & Hurst, J. W. Science 201, 1223−1225 (1978).
14.	Fukuyo, Y., Watanabe, M. M. & Watanabe, M. in Eutrophication and Red Tides in the Coastal Marine Environment 43−52 (National Institute (Japan) for Environmental Studies, Tsukuba, 1982).
15.	Anderson, D. M. & Morel, F. M. M. Estuar. coast. mar. Sci. 8, 279−293 (1979).
16.	Konopka, R. J. & Benzer, S. Proc. natn. Acad. Sci. U.S.A. 68, 2112 (1971). | ChemPort |
17.	Wall, D. & Dale, B. Micropaleontology 14, 265−304 (1968).
18.	Guillard, R. R. L. & Ryther, J. H. Can. J. Microbiol. 8, 229−239 (1962). | PubMed | ISI | ChemPort |