No abstract

It has been predicted that the Arctic Ocean will sequester much greater amounts of carbon dioxide (CO2) from the atmosphere as a result of sea ice melt and increasing primary productivity. However, this prediction was made on the basis of observations from either highly productive ocean margins or ice-covered basins before the recent major ice retreat. We report here a high-resolution survey of sea-surface CO2 concentration across the Canada Basin, showing a great increase relative to earlier observations. Rapid CO2 invasion from the atmosphere and low biological CO2 drawdown are the main causes for the higher CO2, which also acts as a barrier to further CO2 invasion. Contrary to the current view, we predict that the Arctic Ocean basin will not become a large atmospheric CO2 sink under ice-free conditions.

Distributions of total alkalinity (TA), dissolved inorganic carbon (DIC), and other parameters relevant to the marine inorganic carbon system were investigated in shelf and adjacent ocean waters during a U.S. Gulf of Mexico and East Coast Carbon cruise in July-August 2007. TA exhibited near-conservative behavior with respect to salinity. Shelf concentrations were generally high in southern waters (Gulf of Mexico and East Florida) and decreased northward from Georgia to the Gulf of Maine. DIC was less variable geographically and exhibited strongly nonconservative behavior. As a result, the ratio of TA to DIC generally decreased northward. The spatial patterns of other CO 2 system parameters closely followed those of the TA : DIC ratio. All sampled shelf waters were supersaturated with respect to aragonite (saturation state V A . 1). The most intensely buffered and supersaturated waters (V A . 5.0) were in northern Gulf of Mexico river-plume waters; the least intensely buffered and least supersaturated waters (V A , 1.3) were in the deep Gulf of Maine. Due to their relatively low pH, V A , and buffer intensity, waters of the northeastern U.S. shelves may be more susceptible to acidification pressures than are their southern counterparts. In the Mid-Atlantic Bight, alongshore mixing tended to increase DIC concentrations southward, but this effect was largely offset by the opposing effects of biogeochemical processing. In the Gulf of Mexico, downstream increases in Loop Current DIC suggested significant contributions from shelf and gulf waters, estimated at 9.1 3 10 9 mol C d 21 . Off the southeastern U.S., along-flow chemical changes in the Florida Current were dominated by mixing associated with North Atlantic subtropical recirculation.

The combined effects of anthropogenic and biological CO2 inputs may lead to more rapid acidification in coastal waters compared to the open ocean. It is less clear, however, how redox reactions would contribute to acidification. Here we report estuarine acidification dynamics based on oxygen, hydrogen sulfide (H2S), pH, dissolved inorganic carbon and total alkalinity data from the Chesapeake Bay, where anthropogenic nutrient inputs have led to eutrophication, hypoxia and anoxia, and low pH. We show that a pH minimum occurs in mid-depths where acids are generated as a result of H2S oxidation in waters mixed upward from the anoxic depths. Our analyses also suggest a large synergistic effect from river–ocean mixing, global and local atmospheric CO2 uptake, and CO2 and acid production from respiration and other redox reactions. Together they lead to a poor acid buffering capacity, severe acidification and increased carbonate mineral dissolution in the USA’s largest estuary.