Changes in iron supply to oceanic plankton are thought to have a significant effect on concentrations of atmospheric carbon dioxide by altering rates of carbon sequestration, a theory known as the 'iron hypothesis'. For this reason, it is important to understand the response of pelagic biota to increased iron supply. Here we report the results of a mesoscale iron fertilization experiment in the polar Southern Ocean, where the potential to sequester iron-elevated algal carbon is probably greatest. Increased iron supply led to elevated phytoplankton biomass and rates of photosynthesis in surface waters, causing a large drawdown of carbon dioxide and macronutrients, and elevated dimethyl sulphide levels after 13 days. This drawdown was mostly due to the proliferation of diatom stocks. But downward export of biogenic carbon was not increased. Moreover, satellite observations of this massive bloom 30 days later, suggest that a sufficient proportion of the added iron was retained in surface waters. Our findings demonstrate that iron supply controls phytoplankton growth and community composition during summer in these polar Southern Ocean waters, but the fate of algal carbon remains unknown and depends on the interplay between the processes controlling export, remineralisation and timescales of water mass subduction.

In laboratory experiments we examined the interplay of light and iron availability on the intracellular iron concentrations, specific growth rates, and photosynthetic physiology of Southern (S.) Ocean diatoms (Eucampia antarctica and Proboscia inermis) and the haptophyte Phaeocystis antarctica. Intracellular iron concentrations and iron : carbon (Fe : C) molar ratios increased with decreasing irradiance in temperate coastal (Thalassiosira weissflogii) and oceanic (Thalassiosira oceanica) diatoms, in support of the well-established antagonistic iron-light relationship. In contrast, S. Ocean species required lower cellular iron concentrations and Fe : C ratios than temperate diatoms to grow at comparable rates, and their iron requirements decreased or remained relatively constant with decreasing light. These results suggest that the current paradigm that low light increases algal cellular iron requirements (supplied through ''biodilution'') is not applicable to S. Ocean phytoplankton. Although iron use efficiencies decreased at sub-saturating light in all species, these reductions were due primarily to lower growth rates, but not higher intracellular Fe : C ratios, in S. Ocean species. We propose that S. Ocean species have overcome the antagonistic iron-light relationship by increasing the size, rather than the number, of photosynthetic units under low irradiances, resulting in an acclimation strategy that does not increase their cellular iron requirements.

We report results of laboratory studies examining the effect of low levels of iron (Fe) availability on the intracellular Fe concentrations and specific growth rates in Southern Ocean diatoms (Fragilariopsis kerguelensis, Eucampia antarctica, Proboscia inermis, and Thalassiosira antarctica) and Phaeocystis antarctica.

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[1] Platelet ice is the name given to ice crystals that nucleate in the ocean and grow either at depth or loosely attached to the ice-water interface. Related to the proximity of ice shelves, it is known to form in supercooled seawater. This study details the conditions for its growth during the austral winter of 2003 in McMurdo Sound, Antarctica. A key finding is that the presence of platelet ice in the sea ice cover is conclusively linked to the time history of the appearance of ice crystals in the water column, monitored using the strength of the backscattered signal from an acoustic Doppler current profiler as a proxy. Generally, these crystals appeared from mid-May as water near the interface became supercooled. This near-surface supercooling appears to be related to a simultaneous, abrupt change in the structure of the upper 250 m of the water column, from one that behaved dynamically and contained both the warmest and coolest measured temperatures to one in which the water was essentially isothermal near its surface freezing temperature. Near-surface ocean temperature was also affected by tidal mixing and by an increase in the thickness and density, over the course of winter, of the surface mixed layer created by salt rejection during ice growth. These processes allowed cold water, trapped by buoyancy in a band at the base of the mixed layer in early winter, to gain access to the ice-water interface by midwinter. This band of cold water probably had its origin beneath the McMurdo Ice Shelf.