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Physiology of Laminaria
Authors:Nichola J  Conolly Edward A  Drew
Institution:Gatty Marine Laboratory, St. Andrews, Scotland. With 11 figures and 5 tables
Abstract:Abstract. Sporophytes of Laminaria digitata and L. saccharina were collected from the shore at different times of year. Intact sporophytes of both species, and discs cut from L. digitata lamina tissue were maintained for several weeks in laboratory cultures under various nitrate, phosphate, temperature and daylength regimes. Substrate-saturated uptake rates of approximately 24 μgN g dry weight-1 h-1 from 20 μM nitrate and 8 μgP g dry weight-1 h-1 from 10 μM phosphate were more than sufficient to account for internal nitrogen and phosphorus accumulation. Other nitrogen sources - nitrite, ammonium and urea - were also taken up, independently of each other, and supported growth. During the late spring decline of ambient nutrient levels, when growth rates on the shore also decline markedly, enrichment with nitrate (15 μM) and phosphate (3μ) together prevented this decline and also maintained peak photosynthetic rates (net photosynthesis = 10.4 μlO2 cm-2 h-1) which otherwise dropped to 4.5 μO2 cm-2 h-1 over 47 days at ambient nutrient levels (0.5 μM nitrate and phosphate). Slow summer growth rates in June/July were enhanced to greater than spring peak values by combined nitrate (7.5 μM) and phosphate (1.8 μM) enrichment; neither was sufficient alone, although the individual nutrients were accumulated internally. A lesser, but significant enhancement was also achieved in September. In midwinter, nutrient enhancement itself (10.5 μM nitrate and 3.0 μM phosphate) had a small effect on growth rates only if summer water temperature (15°C) was used, but the dramatic effect of an increased photoperiod (7.5 to 17.5 h) was in excess of that expected for the increased radiant energy available. This was found to be due, at least in L. digitaia discs, to the re-establishment of a surface meristoderm in the dormant winter tissue; this was particularly active with high phosphate supply. Growth of the new lamina in January on the shore was much reduced if the old lamina was removed, although the time of initiation of new growth remained unchanged. In the laboratory, the old lamina was found to be a source of nitrogen for new lamina but not of fixed carbon or phosphorus. New lamina photosynthesis, manifest as mannitol accumulation, was directly proportional to phosphate supply up to at least 7.5 μM phosphate. Mannitol accumulation was then suppressed by a nitrate supply above 12 um, presumably by diversion of fixed carbon to other biosynthetic pathways.
Keywords:Laminaria  L  digitata  L  saccharina  laboratory cultures  growth  dissolved nutrients  internal nitrogen and phosphorus  mannitol  daylength  photosynthesis
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