Skip to main content
Log in

Seasonal microbial activity in Antarctic freshwater lake sediments

  • Published:
Polar Biology Aims and scope Submit manuscript

Summary

Seasonal fluctuations in population numbers and activity were monitored in bottom sediments of oligotrophic Moss Lake, mesotrophic Heywood Lake and eutrophic Amos Lake on Signy Island, South Orkney Islands, during 1976–78. Heywood and Amos Lakes became anoxic under winter ice cover (8–10 months) and significant populations of facultatively anaerobic heterotrophs and sulphate-reducing bacteria developed. In contrast, Moss Lake surface sediments never became anoxic and anaerobic bacteria were virtually absent. Direct microscopic counts and viable plate counts fluctuated relatively little in Moss Lake throughout the study period, whereas distinct seasonality was observed in the more enriched lake systems. Similarly, measurements of oxygen consumption and dark 14CO2 uptake by mud cores indicated no obvious seasonal fluctuations in Moss Lake data, in contrast to the marked seasonal pattern observed in data from the other lakes. In these latter systems, oxygen uptake rates were highest in summer (c. 400 mg O2 m-2 d-1) and virtually undetectable in winter. Comparison of oxygen uptake with oxygen concentration and temperature revealed differences, between lakes, in uptake response to oxygen concentration, whereas uptake response to temperature did not differ significantly between lakes. Chemosynthetic production in the Signy Island lake sediments was in the range 1.6–35.3 μg C m-2 (mud surface) d-1 with highest values recorded in Amos Lake under winter ice cover and anoxic conditions. The findings from this and earlier studies of the three lakes have been assembled to indicate the relative importance of green plants and bacteria to the carbon cycle in these permanently cold systems.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Abd-El-Malek Y, Rizk SG (1958) Counting of sulphate-reducing bacteria in mixed bacterial populations. Nature (London) 182:538

    Google Scholar 

  • Allen SE, Grimshaw HM, Parkinson JA, Quarmby C (1974) Chemical analysis of ecological materials. Blackwell, Oxford

    Google Scholar 

  • Burns NM, Ross C (1972) Project Hypo. Canada Centre for Inland Waters, Paper No 6. United States Environmental Protection Agency, Technical Report TS-05-71-208-24

  • Collins VG, Willoughby LG (1962) The distribution of bacteria and fungal spores in Blelham Tarn with particular reference to an experimental overturn. Arch Mikrobiol 43:294–307

    Google Scholar 

  • Collins VG, Jones JG, Hendrie MS, Shewan JM, Wynn-Williams DD, Rhodes ME (1973) Sampling and estimation of bacterial populations in the aquatic environment. In: Board RG, Lovelock DW (eds) Sampling-microbiological monitoring of environments. Academic Press, London New York, pp 77–110

    Google Scholar 

  • Dale NG (1974) Bacteria in intertidal sediments: factors related to their distribution, Limnol Oceanogr 19:509–518

    Google Scholar 

  • Drew EA, Robertson WAA (1974) A simple field version of the Winkler determination of dissolved oxygen. New Phytol 73:793–796

    Google Scholar 

  • Edmondson WT (1966) Changes in oxygen deficit of Lake Washington. Verh Int Verein Theor Angew Limnol 16:153–158

    Google Scholar 

  • Edwards RW, Rolley HLJ (1965) Oxygen consumption of river muds. J Ecol 53:1–19

    Google Scholar 

  • Ellis-Evans JC (1981a) Freshwater microbiology in the Antarctic I —Microbial numbers and activity in oligotrophic Moss Lake. Bull Br Antarct Surv 54:85–104

    Google Scholar 

  • Ellis-Evans JC (1981b) Freshwater microbiology in the Antarctic II —Microbial numbers and activity in mesotrophic Heywood Lake. Bull Br Antarct Surv 54:105–121

    Google Scholar 

  • Fillos J (1977) Effect of sediments on the quality of the overlying water. In: Goltermann HL (ed) Interactions between sediments and fresh water. Proceedings of an international symposium held at Amsterdam, the Netherlands, September 6–10, 1976. Dr. W. Junk BV, The Hague; Centre for Agricultural Publishing and Documentation, Wageningen, pp 266–271

    Google Scholar 

  • Fischer E (1972) A yearly cycle of changes in dynamics of production of the chemoautotrophic bacteria in bottom sediments of a water body. Polskie Arch Hydrobiol 19:343–359

    Google Scholar 

  • Golterman HL (1971) Methods for chemical analyses of fresh waters. Blackwell, Oxford Edinburgh (IBP Handbook No 8)

    Google Scholar 

  • Graneli W (1978) Sediment uptake in South Swedish lakes. Oikos 30:7–16

    Google Scholar 

  • Hargrave BT (1969a) Epibenthic algal production and community respiration in the sediments of Marion Lake. J Fish Res Board Can 26:2003–2026

    Google Scholar 

  • Hargrave BT (1969b) Similarity of oxygen uptake by benthic communities. Limnol Oceanogr 14:801–805

    Google Scholar 

  • Hargrave BT (1972) Aerobic decomposition of sediment and detritus as a function of particle surface area and organic content. Limnol Oceanogr 17:583–596

    Google Scholar 

  • Hargrave BT, (1973) Coupling carbon flow through some pelagic and benthic communities. J Fish Res Board Can 30:1317–1326

    Google Scholar 

  • Herbert RA, Bell CR (1973) Nutrient cycling in freshwater lakes on Signy Island, South Orkney Islands. Bull Br Antarct Surv 37:15–20

    Google Scholar 

  • Heywood RB (1967) The freshwater lakes of Signy Island, South Orkney Islands. I. Catchment areas, drainage systems and lake morphology. Bull Br Antarct Surv 14:25–43

    Google Scholar 

  • Heywood RB (1970) The mouthparts and feeding habits of Parabroteas sarsi (Daday) and Pseudoboeckella silvestri, Daday (Copeopod, Calanoida). In: Holdgate MW (ed) Antarctic ecology, vol 2. Academic Press, London New York, pp 639–650

    Google Scholar 

  • Heywood RB, Dartnall HJG, Priddle J (1979) The freshwater lakes of Signy Island, South Orkney Islands, Antarctica: data sheets. Br Antarct Surv Data 3:1–46

    Google Scholar 

  • Holdgate MW (1964) Terrestrial ecology in the Maritime Antarctic. In: Carrick R, Holdgate MW, Prevost J (eds) Biologie antarctique. Hermann, Paris, pp 181–194

    Google Scholar 

  • Hutchinson GE (1957) A treatise on limonology, vol 1. Geography physics and chemistry. Wiley, New York

    Google Scholar 

  • Jones JG (1976) The microbiology and decomposition of seston in open water and experimental enclosures in a productive lake. J Ecol 64:241–278

    Google Scholar 

  • Jones JG (1980) Some differences in the microbiology of profundal and littoral lake sediments. J Gen Microbiol 117:285–292

    Google Scholar 

  • Jones JG, Simon BM (1975) An investigation of errors in direct counts of aquatic bacteria by epifluoresence microscopy, with reference to a new method for dyeing membrane filters. J Appl Bacteriol 39:317–329

    Google Scholar 

  • Jones JG, Simon BM (1980) Decomposition processes in the profundal region of Blelham Tarn and the Lund Tubes. J Ecol 68:493–512

    Google Scholar 

  • Kalembasa SJ, Jenkinson D (1973) A comparative study of titrimetric and gravimetric methods for the determination of organic carbon in soils. J Sci Food Agric 24:1085–1090

    Google Scholar 

  • Light JJ (1976) An unusual drainage system in an Antarctic valley. Bull Br Antarct Surv 43:77–84

    Google Scholar 

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

    Google Scholar 

  • Lund JWG, Mackereth FJH, Mortimer CH (1963) Changes in depth and time of certain physical and chemical conditions and a standing crop of Asterionella formosa Hass. in the North Basin of Windermere in 1947. Philos Trans R Soc Ser B 246:255–290

    Google Scholar 

  • Mathews DH, Maling DH (1967) The geology of the South Orkney Islands. I. Signy Island. Falkland Island Dependencies Survey Scientific Reports, No 25

  • Ohle W (1956) Bioactivity, production and energy utilization of lakes. Limnol Oceanogr 1:139–149

    Google Scholar 

  • Olah J (1974) Number, biomass and production of planktonic bacteria in the shallow lake Balaton. Arch Hydrobiol 73:193–217

    Google Scholar 

  • Parr JF (1969) Nature and significance of inorganic transformations in tile-drained soils. Soils Fert 32:411–415

    Google Scholar 

  • Petr T (1977) Bioturbation and exchange of chemicals in the mud-water interface. In: Golterman HL (ed) Interactions between sediments and freshwater, Proceedings of an international symposium held at Amsterdam, the Netherlands, September 6–10, 1976. Dr. W. Junk BV, The Hague; Centre for Agricultural Publishing and Documentation, Wageningen, pp 216–266

    Google Scholar 

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

    Google Scholar 

  • Priddle J, Dartnall HJG (1978) The biology of an Antarctic aquatic moss community. Freshwater Biol 8:469–480

    Google Scholar 

  • Romanenko VI (1964) Heterotrophic assimilation of CO2 by bacterial flora of water. Microbiology 3:610–614

    Google Scholar 

  • Rudd JWM, Hamilton RD (1978) Methane cycling in a eutrophic shield lake and its effects on whole lake metabolism. Limnol Oceanogr 23:337–348

    Google Scholar 

  • Skerman, VBD (1967) A guide to the identification of the genera of bacteria. Williams & Wilkins, Baltimore

    Google Scholar 

  • Smith RIL (1972) Vegetation of the South Orkney Islands with particular reference to Signy Island. Br Antarct Surv Sci Rep No 68

  • Sorokin Yu I (1955) On bacterial chemosynthesis in mud deposits. Mikrobiol 24:393–399

    Google Scholar 

  • Sorokin Yu I (1964) On the trophic role of chemosynthesis in water bodies. Int Rev Gesamten Hydrobiol 49:307–324

    Google Scholar 

  • Sorokin Yu I (1970) Interrelations between sulphur and carbon turnover in meromictic lakes. Arch Hydrobiol 66:391–446

    Google Scholar 

  • Sorokin Yu I, Kadota H (1972) Techniques for the assessment of microbial production and decomposition in fresh waters. Blackwell, Oxford Edinburgh (IBP Handbook No 23)

    Google Scholar 

  • Stanley SO, Rose AH (1967) Bacteria and yeasts from lakes on Deception Island. Philos Trans R Soc Ser B 252:199–207

    Google Scholar 

  • Waksman SA (1936) Humus. Williams & Wilkins, Baltimore

    Google Scholar 

  • Welch HE, Kalff J (1974) Benthic photosynthesis and respiration in Char Lake. J Fish Res Board Can 31:609–620

    Google Scholar 

  • Winberg GG (1971) Symbols units and conversion factors in studies of freshwater productivity. IBP (PF) Pamphlet, International Biological Programme Central Office, London

    Google Scholar 

  • Winfrey MR, Zeikus JG (1977) Effect of sulphate on carbon and electron flow during microbial methanogenesis in freshwater sediments. Appl Environ Microbiol 33:275–281

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Ellis-Evans, J.C. Seasonal microbial activity in Antarctic freshwater lake sediments. Polar Biol 1, 129–140 (1982). https://doi.org/10.1007/BF00286999

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00286999

Keywords

Navigation