Carbon and nitrogen content of Laminaria saccharina in the eastern English Channel: biometrics and seasonal variations
François GévaertDominique DavoultAnne CréachRobert KlingMarie‐Andrée JanquinLaurent SeurontYves Lemoine
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Abstract:
Fresh weight (FW), dry weight (DW), carbon and nitrogen content were measured for specimens of Laminaria saccharina (Heterokontophyta: Phaeophyceae) sampled in the eastern English Channel in order to conduct a biometrical study. The aim was to relate carbon and nitrogen masses of the algae to a simple and rapid morphological measurement of the total length of the sporophyte. These relationships were highly significant and appeared very useful to express the standing biomass of L. saccharina in terms of carbon or nitrogen and then to consider dynamic processes such as primary production. Variations in tissue carbon (C) and nitrogen (N) were examined over a complete seasonal cycle. Average carbon and nitrogen content ranged from 23·9 to 31·4% and 2·23 to 3·42% of the total dry weight, respectively. Variations in C/N ratio showed a clear seasonal pattern with an increase in the early spring corresponding to strong photosynthesis and growth.Keywords:
Saccharina
Dry weight
Sporophyte
Carbon fibers
In previous studies, Laminaria saccharina L. (Lamour.) sporophytes were found to exhibit two major peaks of sporogenesis and an annual life cycle in Long Island Sound, New York. Young sporophytes were observed shortly after the sporogenesis peaks in early autumn and spring, but most of the mature sporophytes decayed during summer. A new study was conducted to determine if the spring sporogenesis activity contributed to the recruitment observed in autumn through oversummering of gametophytic and juvenile sporophytic stages, as previously suggested. Reproduction and growth in gametophytes and growth in juvenile sporophytes were studied under crossed gradients of light and temperature. Periodic outplantings of substrata seeded with gametophytic and sporophytic stages to the field were conducted to assess actual survival.
The optimum temperature and light conditions for gametophyte development, growth and reproduction varied with the time of year meiospores were obtained. Most of this variation was attributable to temperature. A seasonal adaptation to temperature in most developmental stages was observed. Higher temperatures resulted in greater numbers of male gametophytes. Gametophytic stages could develop at all times, suggesting that oversummering in this stage was possible. Juvenile sporophytes had a narrower optimum temperature range and again photon fluence rate contributed little to observed variances. Out planting of sporophytic stages at various times during the year indicated only sporophytes prepared from autumn and winter could survive summer conditions. The thalli of these plants grew rapidly in spring and eroded back to the meristematic region in summer. Most of these plants then quickly became reproductive, resulting in another autumn sporogenesis peak. Gametophytic and sporophytic outplantings prepared from spring meiospores did not survive the summer. Thus, the recruitment observed in autumn can only be the result of the previous autumn's sporogenesis activity. The sporogenous activities of spring and early summer appear to be unimportant, despite the fact that all reproductive indices are superior at those times.
Sporophyte
Saccharina
Laminaria digitata
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SUMMARY Meiospores of Laminaria saccharina labeled with a fluorescent stain were put into the sea and recovered at frequent intervals. They developed into gametophytes which produced gametes throughout the year. Antheridia were produced earlier than oogonia. Gametogenesis was slowest during the late autumn and early winter. On the basis of nutritional studies and the seasonal distribution of nutrients, it was concluded that the rate of gametogenesis was not due to nutrient deficiency but most likely to light. Production of macroscopic sporophytes appeared to be limited by survival of microscopic sporophytes rather than gametogenesis. Macroscopic sporophytes became evident during the late winter and autumn. The greater light and perhaps higher temperatures of summer were suggested as agents limiting macroscopic sporophyte production during this period.
Sporophyte
Saccharina
Antheridium
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Laminaria digitata
Sporophyte
Saccharina
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Sporophyte
Saccharina
Frond
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The production, longevity, growth, regeneration and reproduction of Laminaria saccharina (L.) Lamour. on the Devon and Argyll coasts are described. Bathymetric zone and habitat control the fertility and longevity of the gametophyte and consequently the production of the sporophyte. Sporophytes develop at the higher levels during the winter, early spring, late summer and autumn, and at the lower levels during spring, summer and autumn. Longevity of the sporophyte depends on season of germination, bathymetric zone and habitat. Winter sporophytes rarely persist to maturity. Spring sporophytes form the bulk of all L. saccharina populations except on very sheltered coasts in the sublittoral zone where summer sporophytes may be equally numerous. On the British coast the life-span of a L. saccharina sporophyte does not exceed 3 years.
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Saccharina
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The responses to light and temperature variations of the gametophytes and early sporophytes of Laminaria hyperborean were compared in culture with those of its main competitors in Britain, namely L. digitata, L. saccharina and Saccorhiza polyschides . Some undeveloped gametophytes of all species are able to survive in the dark for at least 80 days.
Laminaria digitata
Saccharina
Sporophyte
Competitor analysis
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Sporophyte
Saccharina
Laminaria digitata
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:Kelp ecology is heavily biased toward the conspicuous sporophyte stage, whereas understanding of the microscopic gametophyte remains limited. Given that kelp gametophytes are known to grow in/on other species of algae, we sought to determine if species-specific polymerase chain reaction could detect kelp gametophytes in situ from coextracted host DNA. Upon verifying our molecular results, we also assessed distributional patterns of the kelp gametophytes according to site, host species, and vertical placement in the intertidal zone. We sampled Chondrus crispus, Mastocarpus stellatus, and Palmaria palmata (Florideophyceae) at Wallace Cove, New Brunswick, Canada, on 13 September 2016, where kelp sporophytes were abundant, and at an adjacent location without obvious sporophyte presence, L'Etete, on 26 September 2016. Species-specific primers were used to assess the presence of Alaria esculenta and Laminaria digitata DNA from coextracted red algal DNA. We successfully amplified kelp DNA from the host tissue of each red algal species, indicating that gametophytes were present at Wallace Cove and L'Etete during the fall of 2016, with significantly less gametophyte presence at L'Etete. Although no significant differences in gametophyte presence occurred according to host species, P. palmata had significantly less gametophyte presence when sampled from its upper range in the intertidal. Microscopy and additional field observations confirmed the presence of brown endophytes in a variety of hosts, including C. crispus and P. palmata. Our study showcases a simple method for detecting kelp gametophytes, with our preliminary results demonstrating that the distributional and ecological range of kelp gametophytes is broader than that of the sporophytic counterparts.
Laminaria digitata
Sporophyte
Saccharina
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Cove
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