Current CaCO3 dissolution at the seafloor caused by anthropogenic CO2.

Oceanic uptake of anthropogenic CO2 leads to decreased pH, carbonate ion concentration, and saturation state with respect to CaCO3 minerals, causing increased dissolution of these minerals at the deep seafloor. This additional dissolution will figure prominently in the neutralization of man-made CO2 However, there has been no concerted assessment of the current extent of anthropogenic CaCO3 dissolution at the deep seafloor. Here, recent databases of bottom-water chemistry, benthic currents, and CaCO3 content of deep-sea sediments are combined with a rate model to derive the global distribution of benthic calcite dissolution rates and obtain primary confirmation of an anthropogenic component. By comparing preindustrial with present-day rates, we determine that significant anthropogenic dissolution now occurs in the western North Atlantic, amounting to 40-100% of the total seafloor dissolution at its most intense locations. At these locations, the calcite compensation depth has risen ∼300 m. Increased benthic dissolution was also revealed at various hot spots in the southern extent of the Atlantic, Indian, and Pacific Oceans. Our findings place constraints on future predictions of ocean acidification, are consequential to the fate of benthic calcifiers, and indicate that a by-product of human activities is currently altering the geological record of the deep sea.

Disparate acidification and calcium carbonate desaturation of deep and shallow waters of the Arctic Ocean.

The Arctic Ocean is acidifying from absorption of man-made CO2. Current predictive models of that acidification focus on surface waters, and their results argue that deep waters will acidify by downward penetration from the surface. Here we show, with an alternative model, the rapid, near simultaneous, acidification of both surface and deep waters, a prediction supported by current, but limited, saturation data. Whereas Arctic surface water responds directly by atmospheric CO2 uptake, deeper waters will be influenced strongly by intrusion of mid-depth, pre-acidified, Atlantic Ocean water. With unabated CO2 emissions, surface waters will become undersaturated with respect to aragonite by 2105 AD and could remain so for ∼600 years. In deep waters, the aragonite saturation horizon will rise, reaching the base of the surface mixed layer by 2140 AD and likely remaining there for over a millennium. The survival of aragonite-secreting organisms is consequently threatened on long timescales.

Comment on "Physical model for the decay and preservation of marine organic carbon".

Rothman and Forney (Reports, 1 June 2007, p. 1325) described a model for the decay of marine organic carbon. However, the enzyme deactivation rates required by their model are too fast compared with available data, and the model fails to explain the similarity in observed decay rate constants from different experiments. Alternative models provide equally good fit to the observed temporal trend in decay rate constants.