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Antarctic sea ice viral dynamics over an annual cycle

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Abstract

Viral abundance, burst sizes, lytic production and temperate phage were investigated in land-fast ice at two sites in Prydz Bay Antarctica (68°S, 77°E) between April and November 2008. Both ice cores and brine were collected. There was no seasonal pattern in viral or bacterial numbers. Across the two sites virus abundances ranged between 0.5 × 105 and 5.1 × 105 viruses ml−1 in melted ice cores and 0.6 × 105–3.5 × 105 viruses ml−1 in brine, and bacterial abundances between 2.7 × 104 and 17.3 × 104 cells ml−1 in melted ice cores and 3.9 × 104–32.5 × 104 cells ml−1 in brine. Virus to bacterium ratios (VBR) showed a clear seasonal pattern in ice cores with lowest values in winter (range 1.2–20.8), while VBRs in brine were lower (0.2–4.9). Lytic viral production range from undetectable to 2.0 × 104 viruses ml−1 h−1 in ice cores with maximum rates in September and November. In brine maximum, lytic viral production occurred in November (1.18 × 104 viruses ml−1 h−1). Low burst sizes were typical (3.94–4.03 viruses per bacterium in ice cores and 3.16–4.0 viruses per bacterium in brine) with unusually high levels of visibly infected cells—range 40–50%. This long-term investigation revealed that viral activity was apparent within the sea ice throughout its annual cycle. The findings are discussed within the context of limited data available on viruses in sea ice.

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References

  • Boras JA, Sala MM, Arrieta JM, Sà EL, Felipe J, Agusti S, Duarte CM, Vaqué D (2010) Effect of ice melting on bacterial carbon fluxes channelled by viruses and protists in the Arctic Ocean. Polar Biol 33:1695–1707

    Article  Google Scholar 

  • Borriss M, Helmke E, Hanschke R, Schweder T (2003) Isolation and characterization of marine psychrophilic phage-host systems from Arctic sea ice. Extremophiles 7:377–384

    Article  PubMed  CAS  Google Scholar 

  • Fuhrman JA (1999) Marine viruses and their biogeochemical and ecological effects. Nature 399:541–548

    Article  PubMed  CAS  Google Scholar 

  • Gowing MM (2003) Large viruses and infected micro-eukaryotes in the Ross Sea summer pack ice habitats. Mar Biol 14:1029–1040

    Google Scholar 

  • Gowing MM, Riggs BE, Garrison DL, Gibson AH, Jeffries MO (2002) Large viruses in Ross Sea late autumn pack ice habitats. Mar Ecol Prog Ser 241:1–11

    Article  Google Scholar 

  • Gowing MM, Garrison DL, Gibson AH, Krupp JM, Jeffries MO, Fritsen CH (2004) Bacterial and viral abundance in Ross Sea summer pack ice communities. Mar Ecol Prog Ser 279:3–12

    Article  CAS  Google Scholar 

  • Grossmann S, Dieckmann GS (1994) Bacterial standing stock, activity and carbon production during formation and growth of sea ice in the Weddell Sea, Antarctica. Appl Environ Microbiol 60:2746–2753

    PubMed  CAS  Google Scholar 

  • Guixa-Boixereu N, Vaqué D, Gasol JM, Sánchez-Cámara J, Pedrós-Alió C (2002) Viral distribution and activity in Antarctic waters. Deep Sea Res II 49:827–845

    Article  Google Scholar 

  • Haecky P, Andersson A (1999) Primary and bacterial production in sea ice in the northern Baltic Sea. Aquat Microb Ecol 20:107–118

    Article  Google Scholar 

  • Helmke E, Weyland H (1995) Bacteria in sea ice and underlying water of the eastern Weddell Sea in midwinter. Mar Ecol Prog Ser 287:269–287

    Article  Google Scholar 

  • Hewson IO, O’Neil JM, Fuhrman JA, Dennison WC (2001) Virus like particle distribution and abundance in sediments and overlying waters along eutrophication gradients in two sub-tropical estuaries. Limnol Oceanogr 46:1734–1746

    Article  Google Scholar 

  • Kottmeier ST, Sullivan CW (1987) Late winter primary production and bacterial production in sea ice and seawater west of the Antarctic Peninsula. Mar Ecol Prog Ser 36:287–298

    Article  Google Scholar 

  • Krembs C, Engel A (2001) Abundance and variability of microorganisms and transparent exopolymer particles across the ice-water interface of melting first-year ice in the Laptev Sea (Arctic). Mar Biol 138:173–185

    Article  Google Scholar 

  • Krembs C, Gradinger R, Spindler M (2000) Implications of brine channel geometry and surface for the interaction of sympagic organisms in the Arctic sea ice. J Exp Mar Biol Ecol 243:55–80

    Article  Google Scholar 

  • Laurion I, Demers S, Vézina AF (1995) The microbial food web associated with the ice algal assemblage: biomass and bactivory of nanoflagellates protozoans in Resolute Passage (high Canadian Arctic). Mar Ecol Prog Ser 120:77–87

    Article  Google Scholar 

  • Laybourn-Parry J, Marshall WA, Madan NJ (2007) Viral dynamics and patterns of lysogeny in saline Antarctic lakes. Poar Biol 30:351–358

    Article  Google Scholar 

  • Maranger R, Bird DF (1995) Viral abundance in aquatic systems: a comparison between marine and fresh waters. Mar Ecol Prog Ser 121:217–226

    Article  Google Scholar 

  • Maranger R, Bird DF, Juniper SK (1994) Viral and bacterial dynamics in Arctic sea ice during the spring algal bloom near resolute, NWT, Canada. Mar Ecol Prog Ser 111:121–127

    Article  Google Scholar 

  • Marchant H, Davidson A, Wright S, Glazebrook J (2000) The distribution and abundance of viruses in the Southern Ocean during Spring. Antarctic Sci 12:414–417

    Article  Google Scholar 

  • Meiners K, Brinkmeyer R, Granskog MA, Lindfors A (2004) Abundance, size distribution and bacterial colonization of exoploymer particles in Antarctic sea ice (Bellinghausen Sea). Aquat Microb Ecol 35:283–296

    Article  Google Scholar 

  • Mock T (2002) In situ primary production in young Antarctic sea ice. Hydrobiologia 470:127–132

    Article  CAS  Google Scholar 

  • Noble RT, Fuhrman JA (1997) Virus decay and its causes in coastal waters. Appl Environ Microbiol 63:77–83

    PubMed  CAS  Google Scholar 

  • Noble RT, Fuhrman JA (1998) Use of SYBR Green I for rapid epifluorescence counts of marine viruses and bacteria. Aquat Microb Ecol 14:113–118

    Article  Google Scholar 

  • Pearce I, Davidson AT, Bell EM, Wright S (2007) Seasonal changes in the concentration and metabolic activity of bacteria and viruses at an Antarctic coastal site. Aquat Microb Ecol 47:11–23

    Article  CAS  Google Scholar 

  • Quetin B, Ross RH, Frazer TK, Amsler MO, Watt-Evans C, Oakes SA (2003) Growth of larval krill, Euphasia superba in fall and winter west of the Antarctic Peninsula. Mar Biol 143:833–843

    Article  Google Scholar 

  • Riedel A, Michel C, Gosselin M, LeBlanc B (2007) Enrichment of nutrients, exopolymeric substances and microorganisms in newly formed sea ice on the Mackenzie shelf. Mar Ecol Prog Ser 342:55–67

    Article  CAS  Google Scholar 

  • Ryan KG, Ralph P, McMinn A (2004) Acclimation of Antarctic bottom-ice algal communities to lowered salinites during melting. Polar Biol 27:679–686

    Article  Google Scholar 

  • Säwström C, Granéli W, Laybourn-Parry J, Anesio AM (2007) High viral infection rates in Antarctic and Arctic bacterioplankton. Environ Microbiol 9:250–255

    Article  PubMed  Google Scholar 

  • Smith REH, Clement P, Cota GF (1989) Population dynamics of bacteria in Arctic sea ice. Microbial Ecol 17:63–76

    Article  Google Scholar 

  • Smith DC, Steward GF, Azam F, Hollibaugh JT (1992) Virus and bacterial abundances in the Drake Passage during January and August 1991. Antarctic J US 27:125–127

    Google Scholar 

  • Steward GF, Smith DG, Azam F (1996) Abundance and production of bacteria and viruses in the Bering and Chukchi Seas. Mar Ecol Prog Ser 87:105–112

    Google Scholar 

  • Stoecker DK, Buck KR, Putt M (1993) Changes in the sea ice brine community during spring-summer transition, McMurdo Sound, Antarctica II. Phagotrophic protists. Mar Ecol Prog Ser 95:103–113

    Article  Google Scholar 

  • Thomas DN, Dieckmann GS (2002) Antarctic sea ice—a habitat for extremophiles. Science 295:641–644

    Article  PubMed  CAS  Google Scholar 

  • Thomas DN, Papadimitriou S (2003) Biogeochemistry of sea ice. In: Thomas DN, Dieckmann GS (eds) Sea ice-an introduction to its physics, chemistry, biology and geology. Blackwell, Oxford, pp 267–302

    Google Scholar 

  • Thomas DN, Lara RJ, Haas C, Schnack-Schiel E-M, Dieckmann GS, Kattner G, Nöthig SB, Mizdalski E (1998) Biological soup within decaying summer sea ice in the Amundsen Sea, Antarctica. In: Lizotte MP, Arrigo RK (eds) Antarctic sea ice biological processes, interactions and variability. Antarctic Research Series, 73 American Geophysical Union, Washington DC, pp 161–171

  • Thomson P, McMinn A, Kiessling I, Watson M, Goldsworthy PM (2006) Composition and succession of dinoflagellates and chrysophytes in the upper fast ice off Davis Station, East Antarctica. Polar Biol 29:337–347

    Article  Google Scholar 

  • Weinbauer MG (2004) Ecology of prokaryote viruses. FEMS Microbiol Rev 28:127–181

    Article  PubMed  CAS  Google Scholar 

  • Weinbauer MG, Suttle CA (1996) Potential significance of lysogeny to bacteriophage production and bacterial mortaility in coatal water of the Gulf of Mexico. Appl Environ Microbiol 62:4374–4380

    PubMed  CAS  Google Scholar 

  • Weinbauer MG, Brettar I, Höfle MG (2003) Lysogeny and virus induced mortality of bacterioplankton in surface, deep and anoxic marine waters. Limnol Oceanogr 48:1457–1465

    Article  Google Scholar 

  • Wilhelm SW, Brigden S, Suttle CA (1998) The role of viruses in organic carbon cycling in the sea. Eos 79:OS168

    Google Scholar 

Download references

Acknowledgments

The work was funded by grants form the Australian Antarctic Advisory Committee and the University of Tasmania to JL-P. The authors are indebted to the Davis Station personnel during 2007–2008 who provided logistic support in the field. We thank the Australian Antarctic Division for the use of their Electron Microscopy facilities.

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Correspondence to Johanna Laybourn-Parry.

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Paterson, H., Laybourn-Parry, J. Antarctic sea ice viral dynamics over an annual cycle. Polar Biol 35, 491–497 (2012). https://doi.org/10.1007/s00300-011-1093-z

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