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The seasonal dynamics of Spirogyra in a shallow, maritime Antarctic lake

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Summary

The filamentous chlorophyte Spirogyra forms a mat covering extensive areas of Spirogyra Lake, a small, shallow, Antarctic lake. It has an annual growth pattern, with a maximum standing crop of 400 μg chlorophyll-α m-2 during the ice-free summer period. Nutrient concentrations were low and there was evidence for P-limitation. The attainment of such a high standing crop was probably dependent on the lake's high specific dilution rate. Radiation flux was very low under winter ice cover and Spirogyra died back almost completely. The lake water became hypoxic and inorganic nutrients accumulated in both the water column and overwintering algal filaments. Spore formation was not observed, but changes in the composition of filaments indicated that polysaccharides, which had accumulated in summer, were depleted over the long, ice-covered winter period.

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References

  • Amenta JS (1964) A rapid chemical method for quantification of lipids separated by thin layer chromatography. J Lipid Res 5:270–273

    Google Scholar 

  • Auer MA, Graham JM, Graham LE, Kranzfelder JA (1983) Factors regulating the spatial and temporal distributions of Cladophora and Ulothrix in the Laurentian Great Lakes. In: Wetzel RG (ed) Periphyton of freshwater ecosystems. Junk, The Hague, pp 135–145

    Google Scholar 

  • Bartlett GR (1959) Phosphorus assay in column chromatography. J Biochem 234:466–468

    Google Scholar 

  • Cattaneo A (1987) Periphyton in lakes of different trophy. Can J Fish Aquat Sci 44:296–303

    Google Scholar 

  • Chaney AL, Marbach EP (1962) Modified reagents for the determination of urea and ammonia. Clin Chem 8:71–76

    Google Scholar 

  • Church M (1975) Electrochemical and fluorometric tracer techniques for stream flow measurements. Tech Bull Br Geomorph Res Group No 12

  • Collyer DM, Fogg GE (1955) Studies on fat accumulation in algae. J Exp Bot 6:256–275

    Google Scholar 

  • Cook JR (1963) Adaptions in growth and division in Euglena effected by energy supply. J Protozool 10:436–444

    Google Scholar 

  • Dawson FH (1981) An inexpensive photosynthetic irradiance sensor for ecological field studies. Hydrobiologia 77:71–76

    Google Scholar 

  • Dubois M, Gilles KA, Hamilton JK, Rebers PA, Smith F (1956) Colorimetric method for determination of sugars and related substances. Anal Chem 28:350–354

    Google Scholar 

  • Eisenreich SJ, Bannerman RT, Armstrong DE (1975) A simplified phosphorus analysis technique. Environ Lett 9:43–53

    Google Scholar 

  • Ellis-Evans JC (1985) Decomposition processes in maritime Antarctic lakes. In: Siegfried W, Condy PR, Laws RM (eds) Antarctic nutrient cycles and food webs. Springer, Berlin, pp 253–260

    Google Scholar 

  • Erben K (1962) Sporulation. In: Lewin RA (ed) Physiology and biochemistry of algae. Academic Press, London New York, pp 701–710

    Google Scholar 

  • Forsberg C, Ryding SO, Claesson A, Forsberg A (1978) Water chemical analysis and/or algal assay? Sewage effluent and polluted lake water studies. Mitt Int Verein Limnol 21:352–363

    Google Scholar 

  • Harris GP (1978) Photosynthesis, productivity and growth: The physiological ecology of phytoplankton. Arch Hydrobiol Beih 10:171 pp

    Google Scholar 

  • Hawes I (1983) Nutrients and their effects on phytoplankton populations in lakes on Signy Island, Antarctica. Polar Biol 2:115–126

    Google Scholar 

  • Hawes I (1985) Light climate and phytoplankton photosynthesis in maritime Antarctic lakes. Hydrobiologia 123:69–79

    Google Scholar 

  • Heywood RB (1977) Antarctic freshwater ecosystems: review and synthesis. In: Llano GA (ed) Adaptations within Antarctic ecosystems. Smithsonian Institution, Washington DC, pp 829–837

    Google Scholar 

  • Heywood RB, Dartnall HJG, Priddle J (1980) Characteristics and classification of the lakes of Signy Island, South Orkney Islands, Antarctica. Freshwater Biol 10:47–59

    Google Scholar 

  • Kalff J, Welch HE (1974) Phytoplankton production in Char Lake, a natural polar lake, and in Meretta Lake, a polluted polar lake, Cornwallis Island, Northwest Territories. J Fish Res Board Can 31:621–636

    Google Scholar 

  • Larsen DP, Schults DW, Malueg KW (1981) Summer internal phosphorus supplies in Shagawa Lake, Minnesota. Limnol Oceanogr 26:740–753

    Google Scholar 

  • Lewis MR, Kemp WM, Cunningham JJ, Stevenson JC (1982) A rapid technique for the preparation of aquatic macrophyte samples for measuring 14-C incorporation. Aquat Bot 13:203–207

    Google Scholar 

  • Light JJ, Ellis-Evans JC, Priddle J (1981) Phytoplankton ecology in an Antarctic lake. Freshwater Biol 11:11–26

    Google Scholar 

  • Marker AFH (1980) A note on the extraction of chlorophyll from benthic algae using methanol. Arch Hydrobiol Beih 14:88–90

    Google Scholar 

  • Marker AFH, Nusch EA, Rai H, Riemann B (1980) The measurement of photosynthetic pigments in freshwaters and a standardisation of methods: conclusions and recommendations. Arch Hydrobiol Beih 14:91–106

    Google Scholar 

  • McCracken MD, Gustafson TD, Adams MS (1974) Productivity of Oedogonium in Lake Wingra, Wisconsin. Am Midl Nat 92:247–254

    Google Scholar 

  • Morgan K, Kalff J (1975) The winter survival of an algal flagellate Cryptomonas erosa (Skuja). Verh Int Ver Limnol 19:2734–2740

    Google Scholar 

  • Morris I (1981) Photosynthesis products, physiological state and phytoplankton growth. In: Platt TE (ed) physiological bases of phytoplankton ecology. Can Bull Fish Aquat Sci 210:83–102

  • Morris I, Glover HE, Yentsch CS (1974) Products of photosynthesis by marine phytoplankton: the effect of environmental factors on the relative rates of protein synthesis. Mar Biol 27:1–9

    Google Scholar 

  • Morries P (1971) A note on the ultra-violet spectrophotometric method for the determination of nitrate in water. Water Treat Exam 20:132–137

    Google Scholar 

  • Myers J (1949) The pattern of photosynthesis in Chlorella. In: Franck J and Loomis WE (eds) Photosynthesis in plants. Am Soc Plant Physiol, Iowa State College Press, pp 349–364

  • Mykelstad S (1974) Production of carbohydrates by marine planktonic organisms. I. Comparison of nine different species in culture. J Exp Mar Biol Ecol 15:261–274

    Google Scholar 

  • O'Neal SW, Lembi CA, Spencer DF (1985) Productivity of the filamentous alga Pithophora oedogonia (Chlorophyta) in Surrey Lake, Indiana. J Phycol 21:162–176

    Google Scholar 

  • Palmisano AC, Sullivan CW (1982) Physiology of sea ice diatoms. II. Dark survival of three polar diatoms. Can J Microbiol 29:157–160

    Google Scholar 

  • Priddle J (1980a) The production ecology of benthic plants in some Antarctic lakes. I. In situ production studies. J Ecol 68:141–153

    Google Scholar 

  • Priddle J (1980b) The production ecology of benthic plants in some Antarctic lakes. II. Laboratory physiology studies. J Ecol 68:155–166

    Google Scholar 

  • Priddle J, Hawes I, Ellis-Evans JC (1986) Antarctic aquatic ecosystems as habitats for phytoplankton. Biol Rev 61:199–238

    Google Scholar 

  • Reynolds CS (1984) The ecology of freshwater phytoplankton. Cambridge University Press, Cambridge, 384 pp

    Google Scholar 

  • Rhee G-Y (1978) Effects of N:P atomic ratios and nitrate limitation on algal growth, cell composition and nitrate uptake. Limnol Oceanogr 23:10–25

    Google Scholar 

  • Rhee G-Y, Gotham IJ (1980) Optimum N:P ratios and coexistence of planktonic algae. J Phycol 16:486–489

    Google Scholar 

  • Richardson K, Beardall J, Raven JA (1983) Adaptations of unicellular algae to irradiance: an analysis of strategies. New Phytol 93:157–191

    Google Scholar 

  • Senft WH (1978) Dependence of light-saturated rates of algal photosynthesis on intracellular concentrations of phosphorus. Limnol Oceanogr 23:709–718

    Google Scholar 

  • Smith AE, Morris I (1980) Pathways of carbon assimilation in phytoplankton from the Antarctic Ocean. Limnol Oceanogr 25:865–872

    Google Scholar 

  • Smith RIL (1984) Terrestrial plant ecology of the sub-Antarctic and Antarctic. In: Laws RM (ed) Antarctic ecology. Academic Press, London, pp 61–162

    Google Scholar 

  • Steeman Nielsen E (1962) On the maximum quantity of plankton chlorophyll per surface unit of a lake or sea. Int Rev Hydrobiol 47:335–338

    Google Scholar 

  • Talling JF (1973) The application of some electrochemical methods to the measurement of photosynthesis and respiration in freshwater. Freshwater Biol 3:333–362

    Google Scholar 

  • Welch HE (1974) Metabolic rates of arctic Lakes. Limnol Oceanogr 19:65–73

    Google Scholar 

  • Welch HE, Bergmann MA (1985) Winter respiration of lakes at Saqvaqjuac, N.W.T. Can J Fish Aquat Sci 42:521–528

    Google Scholar 

Download references

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  1. British antarctic Survey, Natural Environment Research Council, High Cross Site, Madingley Road, CB3 0ET, Cambridge, UK

    Ian Hawes

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  1. Ian Hawes
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Hawes, I. The seasonal dynamics of Spirogyra in a shallow, maritime Antarctic lake. Polar Biol 8, 429–437 (1988). https://doi.org/10.1007/BF00264719

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  • DOI: https://doi.org/10.1007/BF00264719

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