Phytoplankton blooms over Arctic Ocean continental shelves are thought to be restricted to waters free of sea ice. Here, we document a massive phytoplankton bloom beneath fully consolidated pack ice far from the ice edge in the Chukchi Sea, where light transmission has increased in recent decades because of thinning ice cover and proliferation of melt ponds. The bloom was characterized by high diatom biomass and rates of growth and primary production. Evidence suggests that under-ice phytoplankton blooms may be more widespread over nutrient-rich Arctic continental shelves and that satellite-based estimates of annual primary production in these waters may be underestimated by up to 10-fold.

Abstract. Fossil fuel use, cement manufacture and land-use changes are the primary sources of anthropogenic carbon dioxide (CO 2 ) to the atmosphere, with the ocean absorbing approximately 30 % (Sabine et al., 2004). Ocean uptake and chemical equilibration of anthropogenic CO 2 with seawater results in a gradual reduction in seawater pH and saturation states ( ) for calcium carbonate (CaCO 3 ) minerals in a process termed ocean acidification. Assessing the present and future impact of ocean acidification on marine ecosystems requires detection of the multi-decadal rate of change across ocean basins and at ocean time-series sites. Here, we show the longest continuous record of ocean CO 2 changes and ocean acidification in the North Atlantic subtropical gyre near Bermuda from 1983-2011. Dissolved inorganic carbon (DIC) and partial pressure of CO 2 (pCO 2 ) increased in surface seawater by ∼40 µmol kg −1 and ∼50 µatm (∼20 %), respectively. Increasing Revelle factor (β) values imply that the capacity of North Atlantic surface waters to absorb CO 2 has also diminished. As indicators of ocean acidification, seawater pH decreased by ∼0.05 (0.0017 yr −1 ) and values by ∼7-8 %. Such data provide critically needed multi-decadal information for assessing the North Atlantic Ocean CO 2 sink and the pH changes that determine marine ecosystem responses to ocean acidification.

The Great Calcite Belt (GCB) is a region of elevated surface reflectance in the Southern Ocean (SO) covering~16% of the global ocean and is thought to result from elevated, seasonal concentrations of coccolithophores. Here we describe field observations and experiments from two cruises that crossed the GCB in the Atlantic and Indian sectors of the SO. We confirm the presence of coccolithophores, their coccoliths, and associated optical scattering, located primarily in the region of the subtropical, Agulhas, and Subantarctic frontal regions. Coccolithophore-rich regions were typically associated with high-velocity frontal regions with higher seawater partial pressures of CO 2 (pCO 2 ) than the atmosphere, sufficient to reverse the direction of gas exchange to a CO 2 source. There was no calcium carbonate (CaCO 3 ) enhancement of particulate organic carbon (POC) export, but there were increased POC transfer efficiencies in high-flux particulate inorganic carbon regions. Contemporaneous observations are synthesized with results of trace-metal incubation experiments, 234 Th-based flux estimates, and remotely sensed observations to generate a mandala that summarizes our understanding about the factors that regulate the location of the GCB.

Coccolithophores are an important component of the Earth system, and, as calcifiers, their possible susceptibility to ocean acidification is of major concern. Laboratory studies at enhanced pCO 2 levels have produced divergent results without overall consensus. However, it has been predicted from these studies that, although calcification may not be depressed in all species, acidification will produce "a transition in dominance from more to less heavily calcified coccolithophores" [Ridgwell A, et al., (2009) Biogeosciences 6:2611-2623. A recent observational study [Beaufort L, et al., (2011) Nature 476:80-83] also suggested that coccolithophores are less calcified in more acidic conditions. We present the results of a large observational study of coccolithophore morphology in the Bay of Biscay. Samples were collected once a month for over a year, along a 1,000-km-long transect. Our data clearly show that there is a pronounced seasonality in the morphotypes of Emiliania huxleyi, the most abundant coccolithophore species. Whereas pH and CaCO 3 saturation are lowest in winter, the E. huxleyi population shifts from <10% (summer) to >90% (winter) of the heavily calcified form. However, it is unlikely that the shifts in carbonate chemistry alone caused the morphotype shift. Our finding that the most heavily calcified morphotype dominates when conditions are most acidic is contrary to the earlier predictions and raises further questions about the fate of coccolithophores in a high-CO 2 world.phytoplankton | North Atlantic | climate change C occolithophores contribute between ∼1% and 10% of marine primary production (1), dominate the pelagic calcium carbonate flux (2), and alter ocean albedo (3). Model predictions suggest that, if CO 2 emissions continue unabated, global surface ocean pH will decrease by 0.3-0.5 units by 2100, leading to a halving of the carbonate ion concentration (4). Along with other calcifiers, coccolithophores such as Emiliania huxleyi are considered susceptible to this ocean acidification (OA). This hypothesis is contentious, however, with diverse calcification responses reported for culture experiments. Many experiments on E. huxleyi (the most common coccolithophore) have found depressed calcification at elevated CO 2 concentration and the associated low pH and low CaCO 3 saturation state (Ω) (5-11), whereas others have found elevated calcification (12, 13) or no trend (10). An in-depth discussion on the reasons behind the contrasting results of Riebesell et al. (5) and can be found in refs. 14 and 15. In a recent study, four different strains of E. huxleyi cultured under identical environmental conditions exhibited varying responses to elevated CO 2 (16), as was also found between coccolithophore species (17).Laboratory studies are unrealistic in many respects and, because of their typically short timescales, preclude the possibility of evolutionary adaptation to the imposed change, a key uncertainty in OA research (17-19). It is therefore vital to complement laboratory experiments with observ...