|Phytoplankton models and life history strategies|
Eilertsen, H.; Wyatt, T. (2000). Phytoplankton models and life history strategies. S. Afr. J. Mar. Sci./S.-Afr. Tydskr. Seewet. 22: 323-338
In: South African Journal of Marine Science = Suid-Afrikaanse Tydskrif vir Seewetenskap. Marine & Coastal Management: Cape Town. ISSN 0257-7615, more
Population-dynamics; Interannual variability; Spring bloom; Environmental-factors; Northeast japan; Ocean; Western norway; Nova-scotia
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Phytoplankton models generally do not consider the initial phases of seed stocks and deal only with the vegetative growth phase, ignoring life history strategies. Some quantitatively important diatoms, such as species of Chaetoceros and Skeletonema, have special strategies with respect to the timing of the planktonic phase that cannot be explained purely on the basis of environmental clues. In Norwegian waters and elsewhere, the first Chaetoceros bloom of the growth season usually starts in mid March, initiated by C. socialis. Other Chaetoceros species appear in the water column later. Species of dinoflagellates like Alexandrium also bloom at certain times of the year. In many cases, phytoplankton inocula originate from resuspension of bottom-dwelling spores or cysts rather than from residual planktonic vegetative cells, and it is probable that, in some species, inoculation events are controlled by endogenous biological clocks. The sequential appearance of different Chaetoceros species may be related to day-length-regulated germination of sports. Most Chaetoceros species have few generations, but they appear at opportunistic times in the plankton. In contrast, Skelelonema costatum and Scrippsiella trochoidea appear at any time of the year. Some modelling results can be improved by including the dynamics of phytoplankton seed stocks in the sediments.