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Photobiology of sea ice algae during initial spring growth in Kangerlussuaq, West Greenland: insights from imaging variable chlorophyll fluorescence of ice cores

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Abstract

We undertook a series of measurements of photophysiological parameters of sea ice algae over 12 days of early spring growth in a West Greenland Fjord, by variable chlorophyll fluorescence imaging. Imaging of the ice–water interface showed the development of ice algae in 0.3–0.4 mm wide brine channels between laminar ice crystals in the lower 4–6 mm of the ice, with a several-fold spatial variation in inferred biomass on cm scales. The maximum quantum yield of photosynthesis, F v /F m, was initially low (~0.1), though this increased rapidly to ~0.5 by day 6. Day 6 also saw the onset of biomass increase, the cessation of ice growth and the time at which brine had reached <50 psu and >−2 °C. We interpret this as indicating that the establishment of stable brine channels at close to ambient salinity was required to trigger photosynthetically active populations. Maximum relative electron transport rate (rETRmax), saturation irradiance (E k) and photosynthetic efficiency (α) had also stabilised by day 6 at 5–6 relative units, ~30 μmol photons m−2 s−1 and 0.4–0.5 μmol photons m−2 s−1, respectively. E k was consistent with under-ice irradiance, which peaked at a similar value, confirming that daytime irradiance was adequate to facilitate photosynthetic activity throughout the study period. Photosynthetic parameters showed no substantial differences with depth within the ice, nor variation between cores or brine channels suggesting that during this early phase of ice algal growth cells were unaffected by gradients of environmental conditions within the ice. Variable chlorophyll fluorescence imaging offers a tool to determine how this situation may change over time and as brine channels and algal populations evolve.

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Abbreviations

E d :

Incident downwelling irradiance of PAR (μmol photons m−2 s−1)

E d(λ):

Incident downwelling irradiance at wavelength λ (μmol photons m−2 s−1 nm−1)

E i :

Downwelling irradiance of PAR immediately under the snow and ice cover (μmol photons m−2 s−1)

E k :

Irradiance above which photosynthesis is light saturated (μmol photons m−2)

DIC:

Dissolved inorganic carbon (μmol L−1 or mmol L−1)

F :

Current fluorescence yield of light-adapted sample

F o F m :

Minimal and maximal fluorescence yield of dark-adapted sample, respectively

\( F_{\text{m}}^{\prime} \) :

Maximal fluorescence yield of light-adapted sample

F v :

(F m − F o)

PAR:

Photosynthetically active radiation—defined as within the 400–700 nm waveband (μmol photons m−2 s−1)

PSI and PSII:

Photosystems I and II

rETR and rETRmax :

Relative rate of electron transport between PSII and PSI (units), and maximum thereof

RLC:

Rapid light curve

Y(II):

\( \left( {F_{\text{m}}^{\prime}-F} \right)/F_{\text{m}}^{\prime} \) quantum yield of PSII under prescribed irradiance

α:

Slope of irradiance versus rETR as irradiance approaches zero ((μmol photons m−2 s−1)−1)

σa :

The absorption cross section area of photosynthetic pigments

References

  • Arrigo KR (2003) Primary production in sea ice. In: Thomas DN, Dieckmann GS (eds) Sea ice: an introduction to its physics, biology, chemistry, and geology. Blackwell, Oxford, pp 143–183

    Google Scholar 

  • Arrigo KR, Thomas DN (2004) Large scale importance of sea ice biology in the Southern Ocean. Ant Sci 16:471–486

    Article  Google Scholar 

  • Arrigo KR, Lizotte MO, Worthen DL, Dixon P, Dieckmann G (1997) Primary production in Antarctic sea ice. Science 276:394–397

    Article  PubMed  CAS  Google Scholar 

  • Baker NR (2008) Chlorophyll fluorescence: a probe of photosynthesis in vivo. Ann Rev Plant Biol 9:89–113

    Article  Google Scholar 

  • Bates S, Cota GF (1986) Fluorescence induction and photosynthesis responses of Arctic ice algae to sample treatment and salinity. J Phycol 26:399–411

    Google Scholar 

  • Cota G, Prinsenberg S, Bennett E, Loder J, Lewis M, Anning J, Watson N, Harris L (1987) Nutrient flux during extended blooms of Arctic ice algae. J Geophys Res 92:1951–1962

    Article  CAS  Google Scholar 

  • Cox GFN, Weeks WF (1983) Equations for determining the gas and brine volumes in sea–ice samples. J Glaciol 29:306–316

    Google Scholar 

  • Eicken H (2003) From the microscopic, to the macroscopic, to the regional scale: growth, microstructure, and properties of sea ice. In: Thomas DN, Dieckmann GS (eds) Sea ice—an introduction to its physics, chemistry, biology and geology. Blackwell Science, Oxford, pp 22–81

    Google Scholar 

  • Eicken H, Bock C, Wittig R, Miller H, Poertner H-O (2000) Magnetic resonance imaging of sea–ice pore fluids: methods and thermal evolution of pore microstructure. Cold Regi Sci Technol 31:207–225

    Article  Google Scholar 

  • Falkowski PG, Raven JA (2007) Aquatic photosynthesis. Princeton University Press, Princeton

    Google Scholar 

  • Glud RN, Rysgaard S, Kühl M (2002) A laboratory study on O2 dynamics and photosynthesis in ice algal communities: quantification by microsensors, O2 exchange rates, 14C incubations and a PAM fluorometer. Aquat Microb Ecol 27:301–311

    Article  Google Scholar 

  • Gradinger R (2009) Sea-ice algae: major contributors to primary production and algal biomass in the Chukchi and Beaufort Seas during May/June 2002. Deep Sea Res 56:1201–1212

    Google Scholar 

  • Grant WS, Horner RA (1976) Growth responses to salinity variation in four Arctic ice diatoms. J Phycol 12:180–185

    Google Scholar 

  • Grunwald B, Kühl M (2004) A system for imaging variable chlorophyll fluorescence of aquatic phototrophs. Ophelia 58:79–89

    Article  Google Scholar 

  • Harrison PJ, Cota GF, Smith REH (1990) Nitrogen utilization in ice algal communities of Barrow Strait, Northwest Territories, Canada. Mar Ecol Prog Ser 67:275–283

    Article  Google Scholar 

  • Hawes I, Sumner DY, Andersen DT (2011) Legacies of recent environmental change in the benthic communities of Lake Joyce, a perennially ice covered, Antarctic lake. Geobiology 9:394–410

    PubMed  CAS  Google Scholar 

  • Horner R, Ackley SF, Dieckmann GS, Gulliksen B, Hoshiai T, Legendre L, Melnikov IA, Reeburgh WS, Spindler M, Sullivan CW (1992) Ecology of sea ice biota. 1. Habitat, terminology, and methodology. Polar Biol 12:417–427

    Article  Google Scholar 

  • Jassby AD, Platt T (1976) Mathematical formulation of the relationship between photosynthesis and light for phytoplankton. Limnol Oceanogr 21:540–547

    Article  CAS  Google Scholar 

  • Kirst GO, Wiencke C (1995) Ecophysiology of polar algae. J Phycol 31:181–199

    Article  Google Scholar 

  • Krembs C, Eicken H, Deming JW (2011) Exopolymer alteration of physical properties of sea ice and implications for ice habitability and biogeochemistry in a warmer Arctic. Proc Nat Acad Sci. doi:10.1073/pnas.1100701108/

    PubMed  Google Scholar 

  • Kühl M, Glud RN, Borum J, Roberts R, Rysgaard S (2001) Photosynthetic performance of surface-associated algae below sea ice as measured with a pulse-amplitude-modulated (PAM) fluorometer and O2 microsensors. Mar Ecol Prog Ser 223:1–14

    Article  Google Scholar 

  • Lizotte MP (2003) Microbiology of sea ice. In: Thomas DN, Dieckmann GS (eds) Sea ice—an introduction to its physics, chemistry, biology and geology. Blackwell Science, Oxford, pp 184–210

    Google Scholar 

  • Lund-Hansen LC, Andersen TJ, Nielsen MH, Pejrup M (2010) Suspended matter, Chl-a, grain-sizes, and optical properties in the Arctic Fjord-type Estuary Kangerlussuaq, West Greenland during summer. Estuaries Coasts 33:1442–1451. doi:10.1007/s12237-010-9300-7

    Article  CAS  Google Scholar 

  • Manes SS, Gradinger R (2009) Small scale vertical gradients of Arctic ice algal photophysiological properties. Photosynth Res 102:53–66

    Article  PubMed  CAS  Google Scholar 

  • McMinn A, Ashworth C, Ryan K (2000) In situ net primary productivity of an Antarctica fast ice bottom algal community. Aquat Microb Ecol 21:177–185

    Article  Google Scholar 

  • McMinn A, Ryan K, Gademann R (2003) Diurnal changes in photosynthesis of Antarctic fast ice algal communities determined by pulse amplitude modulation fluorometry. Mar Biol 143:359–367

    Article  CAS  Google Scholar 

  • McMinn A, Ryan KG, Ralph PJ, Pankowski A (2007) Spring sea ice photosynthesis, primary production and biomass distribution in eastern Antarctica. Mar Biol 151:985–995

    Article  Google Scholar 

  • Mikkelsen DM, Rysgaard S, Glud RN (2008) Microalgal composition and primary production in Arctic sea ice: a seasonal study from Kobbefjord (Kangerluarsunnguaq), West Greenland. Mar Ecol Prog Ser 369:65–74

    Article  Google Scholar 

  • Mock T, Thomas DN (2005) Recent advances in sea–ice microbiology. Environ Microbiol 7:605–619

    Article  PubMed  CAS  Google Scholar 

  • Mundy C, Ehn J, Barber D, Michel C (2007) Influence of snow cover and algae on the spectral dependence of transmitted irradiance through Arctic landfast first-year sea ice. J Geophys Res 112:C03007

    Article  Google Scholar 

  • Nielsen MH, Erbs-Hansen DR, Knudsen KL (2010) Water masses in Kangerlussuaq, a large fjord in West Greenland: the processes of formation and the associated foraminiferal fauna. Polar Res 29:159–175

    Article  Google Scholar 

  • Ralph PJ, Gademan R (2005) Rapid light curves: A powerful tool to assess photosynthetic activity. Aquat Bot 82:222–237

    Article  CAS  Google Scholar 

  • Ralph P, McMinn A, Ryan KG, Ashworth C (2005) Short-term effect of temperature on the photokinetics of microalgae from the surface layers of Antarctic pack ice. J Phycol 41:763–769

    Article  Google Scholar 

  • Ralph PJ, Ryan KG, Martin A, Fenton G (2007) Melting out of sea ice causes greater photosynthetic stress in algae than freezing in. J Phycol 3:948–956

    Article  Google Scholar 

  • Ryan KG, Tay ML, Martin A, McMinn A, Davy SK (2011) Chlorophyll fluorescence imaging analysis of the responses of Antarctic bottom-ice algae to light and salinity during melting. J Exp Mar Biol Ecol 399:156–161

    Google Scholar 

  • Rysgaard S, Kühl M, Glud RN, Hansen JW (2001) Biomass, production and horizontal patchiness of sea ice algae in a high-Arctic fjord (Young Sound, NE Greenland). Mar Ecol Prog Ser 223:15–26

    Article  Google Scholar 

  • Schnack-Schiel SB (2003) The macrobiology of sea ice. In: Thomas DN, Dieckmann GS (eds) Sea ice. An introduction to its physics, chemistry, biology, and geology. Blackwell, Oxford, pp 211–239

  • Vopel K, Hawes I (2006) Photosynthetic performance of benthic microbial mats in Lake Hoare, Antarctica. Limnol Oceanogr 51:1801–1812

    Article  Google Scholar 

  • Weeks WF, Ackley SF (1986) The growth, structure and properties of sea ice. In: Untersteiner N (ed) The geophysics of sea ice. Plenum Press, New York, NY, NATO ASI Series Ser B Physics, pp 9–164

    Google Scholar 

  • Zhang J, Spitz YH, Steele M, Ashjian C, Campbell R, Berline L, Matrai P (2010) Modeling the impact of declining sea ice on the Arctic marine planktonic ecosystem. J Geophys Res 115:C10015

    Article  Google Scholar 

Download references

Acknowledgements

We are grateful to the staff of Kangerlussuaq International Science Support for logistical assistance and kind hospitality in Greenland and to Julie Jacobi Jonstrup for species identifications. This study was funded by the Carlsberg Foundation.

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Correspondence to Brian K. Sorrell.

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Hawes, I., Lund-Hansen, L.C., Sorrell, B.K. et al. Photobiology of sea ice algae during initial spring growth in Kangerlussuaq, West Greenland: insights from imaging variable chlorophyll fluorescence of ice cores. Photosynth Res 112, 103–115 (2012). https://doi.org/10.1007/s11120-012-9736-7

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