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Spatial-temporal variability of ultraplankton vertical distribution in the Antarctic frontal zones within 60–66°E, 43–46°S

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Abstract

The vertical distribution of heterotrophic bacteria and four ultraphytoplanktonic (<10 µm) groups (Prochlorococcus, Synechococcus, pico- and nanoeukaryotes) was investigated by flow cytometry at three process stations located in three different sub-systems belonging to the Antarctic Circumpolar Current frontal zone and to the Southern Indian Ocean (60–66°E, 43–46°S; ANTARES 4 cruise, January-February 1999): the Subtropical Zone (STZ), the Convergence Zone and the Polar Frontal Zone (PFZ). In each sub-system, short-term variability of cell abundance and flow cytometric parameters (right-angle light scatter and chlorophyll autofluorescence) was assessed through a times series of up to 24 h with a 2 h sampling frequency. The ultraphytoplankton vertical distribution exhibited a high spatial variability, with dominance of Prochlorococcus in the STZ (mean: 762.85×1010 cells m−2), whereas picoeukaryotes (<3 µm) were dominant in the PFZ (55.46×1010 cells m−2), a typically high-nutrient low-chlorophyll zone. Heterotrophic bacteria abundance was maximum (9.84×1013 cells m−2) in the frontal zone, between the Agulhas Front and the Subtropical Front. Nanoeukaryotes showed the largest (up to 80%) variations between two consecutive sampling periods (2 h). Abundance variations could not be assigned to the same water mass during the time series due to the highly variable hydrodynamics of the study area. Trends of short-term abundance variations were opposite between the PFZ (lowest at night) and north of the Subtropical Front (highest at night). The observed spatial and short-term variations illustrate the complexity of the water masses in the Indian sector of the Southern Ocean, and highlight the challenge of extrapolating discrete measurements over space and time for use in evaluating carbon budgets in such dynamic areas.

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References

  • Bautista B, Jiménez-Gomez F (1995) Ultraphytoplankton photoacclimation through flow cytometry and pigment analysis of Mediterranean coastal waters. Sci Mar 60:233–241

    Google Scholar 

  • Binder BJ,DuRand MD (2002) Diel cycles in surface waters of the equatorial Pacific. Deep Sea Res II 49:2601–2617

    Article  Google Scholar 

  • Binder BJ, Chisholm SW, Olson RJ, Frankel SL, Worden AZ (1996) Dynamics of picophytoplankton, ultraphytoplankton and bacteria in the central equatorial Pacific. Deep Sea Res II 43:907–931

    Article  Google Scholar 

  • Blanchot J, Rodier M (1996) Picophytoplankton abundance and biomass in the western tropical Pacific ocean during the 1992 El Niño year: results from flow cytometry. Deep Sea Res I 43:877–895

    Article  Google Scholar 

  • Blanchot J, André J-M, Navarette C, Neveux J (1997) Picophytoplankton dynamics in the equatorial Pacific: diel cycling from flow-cytometer observations. C R Acad Sci Paris 320:925–931

    Article  Google Scholar 

  • Bröckel Kv (1981) The importance of nanoplankton within the pelagic Antarctic ecosystem. Kiel Meeresforsch Sonder 5:61–67

    Google Scholar 

  • Buck KR, Chavez FP, Campbell L (1996) Basin-wide distributions of living carbon components and the inverted trophic pyramid of the central gyre of the North Atlantic Ocean, summer 1993. Aquat Microb Ecol 10:283–298

    Google Scholar 

  • Campbell L, Vaulot D (1993) Photosynthetic picoplankton community structure in the subtropical North Pacific Ocean near Hawaï (station ALOHA). Deep Sea Res I 40:2043–2060

    Article  Google Scholar 

  • Cavender-Bares KK, Karl DM, Chisholm SW (2001) Nutrient gradients in the western North Atlantic Ocean: relationship to microbial community structure and comparison to patterns in the Pacific Ocean. Deep Sea Res I 48:2373–2395

    Article  CAS  Google Scholar 

  • Chisholm SW, Olson RJ, Zettler ER, Goericke R, Waterbury JB, Welschmeyer NA (1988) A novel free-living prochlorophyte abundant in the oceanic euphotic zone. Nature 334:340–343

    Article  Google Scholar 

  • Dandonneau Y, Neveux J (1997) Diel variations of in vivo fluorescence in the eastern equatorial Pacific: an unvarying pattern. Deep Sea Res II 44:1869–1880

    Article  CAS  Google Scholar 

  • Delille D (2003) Seasonal and inter-annual variability of bacterioplankton biomass at station Kerfix, off Kerguelen Islands, Antarctica. Oceanol Acta 26:225–229

    Article  Google Scholar 

  • Detmer AE, Bathmann UV (1997) Distribution patterns of autotrophic pico- and nanoplankton and their relative contribution to algal biomass during spring in the Atlantic sector of the Southern Ocean. Deep Sea Res II:299–320

    Google Scholar 

  • DuRand MD, Olson RJ (1996) Contributions of phytoplankton light scattering and cell concentration change to diel variations in beam attenuation in the equatorial Pacific from flow cytometry measurements of pico-, ultra- and nanoplankton. Deep Sea Res 43:891–906

    Article  Google Scholar 

  • Dusenberry JA, Olson RJ, Chisholm SW (2000) Field observations of oceanic mixed layer dynamics and picophytoplankton photoacclimation. J Mar Syst 24:221–232

    Article  Google Scholar 

  • Dusenberry JA, Olson RJ, Chisholm SW (2001) Photoacclimation kinetics of single-cell fluorescence in laboratory and field populations of Prochlorococcus. Deep Sea Res I 48:1443–1458

    Article  Google Scholar 

  • Fiala M, Semeneh M, Oriol L (1998) Size-fractionated phytoplankton biomass and species composition in the Indian sector of the Southern Ocean during austral summer. J Mar Syst 17:179–194

    Article  Google Scholar 

  • Fiala M, Machado C, Oriol L (2002) Phytoplankton distribution in the Indian sector of the Southern Ocean during spring. Deep Sea Res II 49:1867–1880

    Article  CAS  Google Scholar 

  • Fiala M, Delille B, Dubreuil C, Kopczynska E, Leblanc K, Morvan J, Quéguiner B, Blain S, Cailliau C, Conan P, Corvaisier R, Denis M, Frankignoulle M, Oriol L, Roy S (2003) Mesoscale surface distribution of biogeochemical characteristics associated with a frontal system in the Crozet Basin (Southern Indian Ocean) during austral summer 1999. Mar Ecol Prog Ser 249:1–14

    CAS  Google Scholar 

  • Fouilland E, Descolas-Gros C, Courties C, Pons V (1999) Autotrophic carbon assimilation and biomass from size-fractionated phytoplankton in the surface waters across the subtropical frontal zone (Indian Ocean). Polar Biol 21:90–96

    Article  Google Scholar 

  • Gilmer RW (1974) Some aspects of feeding in thecosomatous pteropod molluscs. J Exp Mar Biol Ecol 15:127–144

    Google Scholar 

  • Gilmer RW (1990) In situ observations of feeding behavior of thecosome pteropod molluscs. Am Malacol Bull 8:53–59

    Google Scholar 

  • Guillard RRL, Kilham P (1977) The ecology of marine planktonic diatoms. The biology of diatoms. University of California Press

  • Hewes CD, Holm-Hansen O, Sakshaug E (1985) Alternate carbon pathways at lower trophic levels in the Antarctic food web. In: Siegfried W, Condy P, Laws R (eds) Antarctic nutrient cycles and food webs. Springer, Berlin Heidelberg New York, pp 277–283

  • Jacques G, Panouse M (1991) Biomass and composition of size fractionated phytoplankton in the Weddell-Scotia Confluence area. Polar Biol 11:315–328

    Google Scholar 

  • Kopczynska E, Fiala M, Jeandel C (1998) Annual and interannual variability in phytoplankton at a permanent station off Kerguelen Islands, Southern Ocean. Polar Biol 20:342–351

    Article  Google Scholar 

  • Landry MR, Kirshtein B (1993) Quantitative enumeration of paraformaldehyde preserved Prochlorococcus by flow cytometry. Signal Noise 6:3

    Google Scholar 

  • Leblanc K, Quéguiner B, Fiala M, Blain S, Morvan J, Corvaisier R (2002) Particulate biogenic silica and carbon production rates and particulate matter distribution in the Indian sector of the Subantarctic Ocean. Deep Sea Res II 49:3189–3206

    Article  CAS  Google Scholar 

  • Li WKW, Wood AM (1988) Vertical distribution of North Atlantic ultraphytoplankton: analysis by flow cytometry and epifluorescence microscopy. Deep Sea Res 35:1615–1638

    Article  Google Scholar 

  • Liu H, Nolla HA, Campbell L (1997) Prochlorococcus growth rate and contribution to primary production in the equatorial and subtropical North Pacific Ocean. Aquat Microb Ecol 12:39–47

    Google Scholar 

  • Loka Bharathi PA, Nair S, De Souza M-JBD, Chandramohan D (2001) Assessment of viability in the bacterial standing stock of the Antarctic sea from the Indian side. Oceanol Acta 24:577–580

    Article  Google Scholar 

  • Mann EL, Chisholm SW (2000) Iron limits the cell division rate of Prochlorococcus in the eastern equatorial Pacific. Limnol Oceanogr 45:1067–1076

    CAS  Google Scholar 

  • Mayzaud P, Tirelli V, Errhif A, Labat JP, Razouls S, Perissinotto R (2002) Carbon intake by zooplankton. Importance and role of zooplankton grazing in the Indian sector of the Southern Ocean. Deep Sea Res 49:3169–3187

    Article  Google Scholar 

  • Metzl N, Tilbrook BD, Poisson A (1999) The annual fCO2 cycle and the air-sea CO2 flux in the sub-Antarctic Ocean. Tellus 51B:849–861

    CAS  Google Scholar 

  • Moore LR, Goericke R, Chisholm SW (1995) Comparative physiology of Synechococcus and Prochlorococcus: influence of light and temperature on growth, pigments, fluorescence and absorptive properties. Mar Ecol Prog Ser 116:259–275

    Google Scholar 

  • Moore LR, Rocap G, Chisholm SW (1998) Physiology and molecular phylogeny of coexisting Prochlorococcus ecotypes. Nature 393:464–467

    PubMed  Google Scholar 

  • Murphy LS, Haugen EM (1985) The distribution and abundance of phototrophic ultraplankton in the North Atlantic. Limnol Oceanogr 30 1:47–58

    Google Scholar 

  • Olson RJ, Chisholm SW, Zettler ER, Armbrust EV (1988) Analysis of Synechococcus pigment types in the sea using single and dual beam flow cytometry. Deep Sea Res 35:425–440

    Article  CAS  Google Scholar 

  • Olson RJ, Chisholm SW, Zettler ER, Altabet MA, Dusenberry JA (1990a) Spatial and temporal distributions of prochlorophyte picoplankton in the North Atlantic Ocean. Deep Sea Res 37:1033–1051

    Article  Google Scholar 

  • Olson RJ, Chisholm SW, Zettler ER, Armbrust EV (1990b) Pigments, size, and distribution of Synechococcus in the North Atlantic and Pacific Oceans. Limnol Oceanogr 35:45–58

    CAS  Google Scholar 

  • Park Y-H (1989) Synthèse sur les caractéristiques du Courant Circumpolaire Antarctique. Ann Hydrogr 763:7–32

    Google Scholar 

  • Park Y-H, Gamberoni L (1997) Cross-frontal exchange of Antarctic Intermediate Water and Antarctic Bottom Water in the Crozet Basin. Deep Sea Res II 44:963–986

    Article  CAS  Google Scholar 

  • Park Y-H, Gamberoni L, Charriaud E (1993) Frontal structure, water masses, and circulation in the Crozet Basin. J Geophys Res 98:12361–12385

    Google Scholar 

  • Park Y-H, Pollard RT, Read JF, Leboucher V (2002) A quasi-synoptic view of the frontal circulation in the Crozet Basin during the Antares-4 cruise. Deep Sea Res II 49:1823–1842

    Article  CAS  Google Scholar 

  • Partensky F, Blanchot J, Lantoine F, Neveux J, Marie D (1996) Vertical structure of picophytoplankton at different trophic sites of the tropical northeastern Atlantic Ocean. Deep Sea Res 43:1191–1213

    Article  CAS  Google Scholar 

  • Partensky F, Blanchot J, Vaulot D (1999a) Differential distribution and ecology of Prochlorococcus and Synechococcus in oceanic waters: a review. Bull Inst Océanogr Monaco (spécial 19)

  • Partensky F, Hess WR, Vaulot D (1999b) Prochlorococcus, a marine photosynthetic prokaryote of global significance. Microbiol Mol Biol Rev:106–127

    Google Scholar 

  • Sedwick PN, Blain S, Quéguiner B, Griffiths FB, Fiala M, Bucciarelli E, Denis M (2002) Resource limitation of phytoplankton growth in the Crozet Basin, Subantarctic Southern Ocean. Deep Sea Res II 49:3327–3349

    Article  Google Scholar 

  • Shalapyonok A, Olson RJ, Shalapyonok LS (2001) Arabian Sea phytoplankton during Southwest and Northeast Monsoons 1995: composition, size structure and biomass from individual cell properties measured by flow cytometry. Deep Sea Res II 47:3181–3200

    Google Scholar 

  • Sherry ND, Wood AM (2001) Phycoerythrin-containing picocyanobacteria in the Arabian Sea in February 1995: diel patterns, spatial variability, and growth rates. Deep Sea Res II 48:1263–1283

    Article  Google Scholar 

  • Trousselier M, Courties C, Zettelmaier S (1995) Flow cytometric analysis of coastal lagoon bacterioplankton and picophytoplankton: fixation and storage effects. Estuarine Coastal Shelf Sci 40:621–633

    Article  Google Scholar 

  • Vaulot D, Marie D (1999) Diel variability of photosynthetic picoplankton in the Equatorial Pacific. J Geophys Res 104:3297–3310

    Article  CAS  Google Scholar 

  • Vaulot D, Partensky F (1991) Photosynthetic picoplankton of the north west Mediterranean Sea in summer: comparison with the winter situation. Water Pollut Res Rep 28:173–181

    Google Scholar 

  • Vaulot D, Courties C, Partensky F (1989) A simple method to preserve oceanic phytoplankton for flow cytometric analysis. Cytometry 10:629–635

    CAS  PubMed  Google Scholar 

  • Vaulot D, Marie D, Olson RJ, Chisholm SW (1995) Growth of Prochlorococcus, a photosynthetic prokaryote, in the equatorial Pacific ocean. Science 268:1480–1482

    CAS  Google Scholar 

  • Verity PG, Robertson CY, Tronzo CR, Andrews MG, Nelson JR, Sieracki ME (1992) Relationship between cell volume and the carbon and nitrogen content of marine photosynthetic nanoplankton. Limnol Oceanogr 37:1434–1446

    CAS  Google Scholar 

  • Weber LH, El-Sayed SZ (1987) Contributions of the net, nano- and picoplankton to the phytoplankton standing crop and primary productivity in the Southern Ocean. J Plankton Res 9:973–994

    Google Scholar 

  • Weeks SJ, Shillington FA (1996) Phytoplankton pigment distribution and frontal structure in the subtropical convergence region south of Africa. Deep Sea Res I 43:739–768

    Article  Google Scholar 

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Acknowledgements

This work is a French contribution to the SO-JGOFS program. It was supported by the French Polar Institute (IPEV) and the INSU-CNRS. We thank the captain, officers and crew of RV "Marion Dufresne" and B. Ollivier for outstanding on-board support. Special thanks go to Y.-H. Park for his advice and stimulating discussions. We are grateful to the anonymous reviewers for their constructive remarks and manuscript improvements.

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Correspondence to Michel Denis.

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Dubreuil, C., Denis, M., Conan, P. et al. Spatial-temporal variability of ultraplankton vertical distribution in the Antarctic frontal zones within 60–66°E, 43–46°S. Polar Biol 26, 734–745 (2003). https://doi.org/10.1007/s00300-003-0545-5

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