Polar Biology

, Volume 16, Issue 1, pp 19–25 | Cite as

Inter-annual variability in marine coastal Antarctic bacterioplankton

  • D. Delille
  • L. Mallard
  • C. Rosiers
Original Paper

Abstract

The dynamics of Antarctic coastal marine bacterioplankton has been studied over a 2-year period. Two field stations were sampled between one and three times a week in 1989 and 1991 in the “Terre Adélie” area. The survey included physicochemical (temperature and particulate organic matter) and bacteriological (total and heterotrophic counts, cell volume and frequency of dividing cells estimation) measurements. The results suggest that a strong interannual variability affects the total bacterial abundance, the mean cell volume, the percentage of free living cells and, to a lesser extent. the culturable saprophytic bacterial communities. The observed variability could be partly explained by a large deficit of solar irradiance during the 2nd year of study that may have affected sea ice and seawater primary production.

Keywords

Organic Matter Bacterial Community Field Station Cell Volume Interannual Variability 

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References

  1. Ackley SF, Buck KR, Taguchi S (1979) Standing crop of algae in the sea ice of the Weddell Sea region. Deep Sea Res 26:269–281Google Scholar
  2. Albright LJ, McCrae SK (1987) Annual cycle of bacterial specific biovolumes in Howe Sound, a Canadian West Coast Fjord Sound. Appl Environ Microbiol 52:2739–2744Google Scholar
  3. Azam F, Hodson RE (1977) Size distribution and activity of marine microheterotrophs. Limnol Oceanogr 22:492–501Google Scholar
  4. Bhakoo M, Herbert RA (1980) Fatty acid and phospholipid composition of five psychrotrophicPseudomonas spp. grown at different temperatures. Arch Microbiol 126:51–55CrossRefPubMedGoogle Scholar
  5. Bölter M, Dawson R (1982) Heterotrophic utilization of biochemical compounds in Antarctic waters. Neth J Sea Res 16:315–332Google Scholar
  6. Caron DA, Davis PG, Sieburth JMcN (1989) Factors responsible for the differences in cultural estimates and direct microscopical counts of populations of bactivorous nanoflagellates. Microb Ecol 18:89–104CrossRefGoogle Scholar
  7. Choi JW, Peters F (1992) Effects of temperature on two psychrophilic ecotypes of a heterotrophic nanoflagellate,Paraphysomonas imperforata. Appl Environ Microbiol 58:593–599PubMedGoogle Scholar
  8. Chrzanowski TH, Crotty RD, Hubbard GJ (1988) Seasonal variation in cell volume of epilimnetic bacteria. Microb Ecol 16:155–163CrossRefGoogle Scholar
  9. Davidson AT, Marchant HJ (1992) Protist abundance and carbon concentration during aPhaeocystis-dominated bloom at an Antarctic coastal site. Polar Biol 12:387–395CrossRefGoogle Scholar
  10. Delille D (1990) Factors affecting the horizontal patchiness of coastal Antarctic seawater bacteria. Polar Biol 11:41–45CrossRefGoogle Scholar
  11. Delille D (1992) Marine bacterioplankton at the Weddell Sea ice edge: distribution of psychrophilic and psychrotrophic populations. Polar Biol 12:205–210CrossRefGoogle Scholar
  12. Delille D (1993) Seasonal changes in the abundance and composition of marine heterotrophic bacterial communities in an Antarctic coastal area. Polar Biol 13:463–470CrossRefGoogle Scholar
  13. Delille D, Bouvy M (1989) Bacterial responses to natural organic inputs in a marine sub-Antarctic area. Hydrobiologia 182:225–238Google Scholar
  14. Delille D, Mallard L (1991) Influence of temperature on the growth potential of southern polar bacteria. Kiel Meeresforsch 8:213–218Google Scholar
  15. Delille D, Perret E (1989) Influence of temperature on the growth potential of southern polar bacteria 18:117–123Google Scholar
  16. Delille D, Bouvy M, Cahet G (1988) Short term variations of bacterioplankton in Antarctic zone: Terre Adélie area. Microb Ecol 15:293–309CrossRefGoogle Scholar
  17. Delille D, Fiala M, Rosiers C (1995) Seasonal changes in phytoplankton and bacterioplankton distribution at the ice-water interface in the Antarctic neritic area. Mar Ecol Prog Ser 123:225–233Google Scholar
  18. Fabiano M, Povero P, Danovaro R (1993) Distribution and composition of particulate organic matter in the Ross Sea (Antarctica). Polar Biol 13:525–533CrossRefGoogle Scholar
  19. Ferguson RL, Rublee P (1976) Contribution of bacteria to coastal microplankton standing crop. Limnol Oceanogr 21:141–145Google Scholar
  20. Fukunaga N, Russell NJ (1990) Membrane lipid composition and glucose uptake in two psychrotolerant bacteria from Antarctica. J Gen Microbiol 136:1669–1673Google Scholar
  21. Garrison DL, Buck KR (1989) The biota of Antarctic pack ice in the Weddell Sea and Antarctic peninsula regions. Polar Biol 10:211–219CrossRefGoogle Scholar
  22. Garrison DL, Buck KR, Fryxell GA (1987) Algal assemblages in Antarctic pack-ice and in ice-edge plankton. J Phycol 23:564–572Google Scholar
  23. Gibson JAE, Garrick RC, Burton HR (1990) The annual cycle of bacterial numbers at an inshore site near the Antarctic continent. Proc NIPR Symp Polar Biol 3:16–22Google Scholar
  24. Gleitz M, Kirst GO (1991) Photosynthesis-irradiance relationships and carbon metabolism of different ice algal assemblages collected from Weddell Sea pack ice during austral spring (EPOS 1). Polar Biol 11:385–392CrossRefGoogle Scholar
  25. Hagström A, Larsson U (1984) Diel and seasonal variation in growth rates of pelagic bacteria. In: Hobbie JE, Williams PR (eds) Heterotrophic activity in the sea Plenum Press, New York pp 249–262Google Scholar
  26. Hagström A, Larsson V, Horsted P, Normark S (1979) Frequency of dividing cells, a new approach to the determination of bacterial growth rates in aquatic environments. Appl Environ Microbiol 37:805–812PubMedGoogle Scholar
  27. Hanson RB, Lowery HK (1985) Spatial distribution, structure, biomass and physiology of microbial assemblages across the Southern Ocean frontal zones during the late austral winter. Appl Environ Microbiol 49:1029–1039PubMedGoogle Scholar
  28. Hobbie JE, Daley RJ, Jasper S (1977) Use of nuclepore filters for counting bacteria by fluorescence microscopy. Appl Environ Microbiol 33:1225–1228PubMedGoogle Scholar
  29. Horner RA, Schrader GC (1982) Relative contribution of ice algae, phytoplankton, and benthic microalgae to primary production in nearshore regions of the Beaufort Sea. Arctic 35:485–503Google Scholar
  30. Karl DM (1993) Microbial processes in the southern oceans. Antarctic Microbiology. Wiley, New York, pp 1–63Google Scholar
  31. Koike I, Holm-Hansen O, Biggs DC (1986) Inorganic nutrient metabolism by Antarctic phytoplankton with special reference to ammonium cycling. Mar Ecol Prog Ser 30:105–116Google Scholar
  32. Kottmeier ST, Sullivan CW (1988) Sea ice microbial communities, 9. Effects of temperature and salinity on rates of metabolism and growth of autotrophs and heterotrophs. Polar Biol 8:293–304CrossRefGoogle Scholar
  33. Kottmeier ST, Grossi M, Sullivan CW (1987) Sea ice microbial communities. VIII. Bacterial production in annual sea ice of McMurdo Sound, Antarctica. Mar Ecol Prog Ser 35:175–186Google Scholar
  34. Kuosa H, Kivi K (1989) Bacteria and heterotrophic flagellates in the pelagic carbon cycle in the northern Baltic Sea. Mar Ecol Prog Ser 53:93–100Google Scholar
  35. Li WKW, Dickie PM (1987) Temperature characteristics of photosynthetic and heterotrophic activities: seasonal variations in temperate microbial plankton. Appl Environ Microbiol 53:2282–2285PubMedGoogle Scholar
  36. Palmisano AC, Sullivan CW (1983) Sea ice microbial communities (SIMCO). 1. Distribution, abundance, and primary production of ice microalgae in McMurdo Sound, Antarctica in 1980. Polar Biol 2:171–177CrossRefGoogle Scholar
  37. Pennock JR, Sharp JH (1986) Phytoplankton production in the Delaware Estuary: temporal and spatial variability. Mar Ecol Prog Ser 34:143–155Google Scholar
  38. Pick FR, Caron DA (1987) Picoplankton and nanoplankton biomass in Lake Ontario: relative contribution of phototrophic and heterotrophic communities. Can J Fish Aquat Sci 44:2164–2172Google Scholar
  39. Pomeroy LR, Deibel D (1986) Temperature regulation of bacterial activity during the spring bloom in Newfoundland coastal waters. Science 233:359–361Google Scholar
  40. Rheinheimer G, Gocke K, Hoppe HG (1989) Vertical distribution of microbiological and hydrographic-chemical parameters in different areas of the Baltic Sea. Mar Ecol Prog Ser 52:55–70Google Scholar
  41. Ronner U, Sorensson F, Holm-Hansen O (1983) Nitrogen assimilation by phytoplankton in the Scotia Sea. Polar Biol 2:137–147Google Scholar
  42. Satoh H, Fukami K, Watanabe K, Takahashi E (1989) Seasonal changes in heterotrophic bacteria under fast ice near Syowa station, Antarctica. Can J Microbiol 35:329–333Google Scholar
  43. Sherr EB, Rassoulzadegan F, Sherr BF (1989) Bacterivory by pelagic chereotrichous ciliates in coastal waters of the NW Meditterranean Sea. Mar Ecol Prog Ser 55:235–240Google Scholar
  44. Smith REH, Clement P (1990) Heterotrophic activity and bacterial productivity in assemblages of microbes from sea ice in the high Arctic. Polar Biol 10:351–357CrossRefGoogle Scholar
  45. Smith REH, Clement P, Cota GF (1989) Population dynamics of bacteria in the Arctic sea ice. Microb Ecol 17:63–76CrossRefGoogle Scholar
  46. Smith WO, Nelson DM (1985) Phytoplankton bloom produced by a receding ice-edge in the Ross Sea: spatial coherence with the density field. Science 227:163–166Google Scholar
  47. Sullivan CW, Palmisano AC (1984) Sea ice microbial communities: distribution, abundance and diversity of ice bacteria in McMurdo Sound, Antarctica in 1980. Appl Environ Microbiol 47:788–795PubMedGoogle Scholar
  48. Tanoue E (1985) Distribution and chemical composition of particulate organic matter in the Pacific sector of the Antarctic Ocean. Trans Tokyo Univ Fish 6:43–57Google Scholar
  49. Unanue M, Ayo B, Azua I, Barnica I, Iriberri J (1992) Temporal variability of attached and free-living bacteria in coastal waters. Microb Ecol 23:27–39CrossRefGoogle Scholar
  50. Vincent WE (1988) Microbial ecosystems of Antarctica. Cambridge University Press, CambridgeGoogle Scholar
  51. Vosjan JH, Olanczuk-Neyman KM (1991) Influence of temperature on respiratory ETS-Activity of micro-organisms from Admiralty Bay, King George Island, Antarctica. Neth J Sea Res 28:221–225Google Scholar
  52. Wiebe M, Sheldon WM, Pomeroy LR (1992) Bacterial growth in the cold: evidence for an enhanced substrate requirement. Appl Environ Microbiol 58:359–364PubMedGoogle Scholar
  53. Wiebe WJ, Sheldon WM, Pomeroy LR (1993) Evidence for an enhanced substrate requirement by marine mesophilic bacterial isolates at minimal growth temperatures. Microb Ecol 25:151–159CrossRefGoogle Scholar

Copyright information

© Springer-Verlag 1996

Authors and Affiliations

  • D. Delille
    • 1
  • L. Mallard
    • 1
  • C. Rosiers
    • 2
  1. 1.Observatoire Océanologique de BanyulsUniversité P. et M. Curie U.A. 117, Laboratoire AragoBanyuls sur merFrance
  2. 2.Université Claude Bernard Lyon 1 Laboratoire d'écologie microbienneVillevrbanneFrance

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