Natural variability in the surface ocean carbonate ion concentration
نویسندگان
چکیده
We investigate variability in the surface ocean carbonate ion concentration ([CO 3 ]) on the basis of a long control simulation with an Earth System Model. The simulation is run with a prescribed, pre-industrial atmospheric CO2 concentration for 1000 years, permitting investigation of natural [CO 3 ] variability on interannual to multi-decadal timescales. We find high interannual variability in surface [CO 3 ] in the tropical Pacific and at the boundaries between the subtropical and subpolar gyres in the Northern Hemisphere, and relatively low interannual variability in the centers of the subtropical gyres and in the Southern Ocean. Statistical analysis of modeled [CO 3 ] variance and autocorrelation suggests that significant anthropogenic trends in the saturation state of aragonite (aragonite) are already or nearly detectable at the sustained, open-ocean time series sites, whereas several decades of observations are required to detect anthropogenic trends in aragonite in the tropical Pacific, North Pacific, and North Atlantic. The detection timescale for anthropogenic trends in pH is shorter than that for aragonite, due to smaller noise-to-signal ratios and lower autocorrelation in pH. In the tropical Pacific, the leading mode of surface [CO 3 ] variability is primarily driven by variations in the vertical advection of dissolved inorganic carbon (DIC) in association with El Niño–Southern Oscillation. In the North Pacific, surface [CO 3 ] variability is caused by circulation-driven variations in surface DIC and strongly correlated with the Pacific Decadal Oscillation, with peak spectral power at 20–30-year periods. North Atlantic [CO 3 ] variability is also driven by variations in surface DIC, and exhibits weak correlations with both the North Atlantic Oscillation and the Atlantic Multidecadal Oscillation. As the scientific community seeks to detect the anthropogenic influence on ocean carbonate chemistry, these results will aid the interpretation of trends calculated from spatially and temporally sparse observations.
منابع مشابه
Southern Ocean acidification: a tipping point at 450-ppm atmospheric CO2.
Southern Ocean acidification via anthropogenic CO(2) uptake is expected to be detrimental to multiple calcifying plankton species by lowering the concentration of carbonate ion (CO(3)(2-)) to levels where calcium carbonate (both aragonite and calcite) shells begin to dissolve. Natural seasonal variations in carbonate ion concentrations could either hasten or dampen the future onset of this unde...
متن کاملChanges in calcification of coccoliths under stable atmospheric CO2
The response of coccolithophore calcification to ocean acidification has been studied in culture experiments as well as in present and past oceans. The response, however, is different between species and strains, and for the relatively small carbonate chemistry changes observed in natural environments, a uniform response of the entire coccolithophore community has not been documented so far. Mo...
متن کاملA Paleo Perspective on the Ocean’s Role in the Carbon Cycle
Recently developed proxies for the seawater carbonate ion concentration were used to reconstruct the vertical gradient in the carbonate ion concentration for times in the past corresponding to the glacialinterglacial cycles. The reconstructed changes leave little doubt that the ocean drove the large natural variations in atmospheric carbon dioxide that accompanied the glacial cycles, most likel...
متن کاملSalinity from space unlocks satellite-based assessment of ocean acidification.
Approximately a quarter of the carbon dioxide (CO2) that we emit into the atmosphere is absorbed by the ocean. This oceanic uptake of CO2 leads to a change in marine carbonate chemistry resulting in a decrease of seawater pH and carbonate ion concentration, a process commonly called ‘Ocean Acidification’. Salinity data are key for assessing the marine carbonate system, and new space-based salin...
متن کاملThe effect of carbonate chemistry on calcification and photosynthesis in the hermatypic coral Acropora eurystoma
The rise in atmospheric CO2 has caused significant decrease in sea surface pH and carbonate ion (CO 22 3 ) concentration. This decrease has a negative effect on calcification in hermatypic corals and other calcifying organisms. We report the results of three laboratory experiments designed specifically to separate the effects of the different carbonate chemistry parameters (pH, CO 22 3 , CO2 [a...
متن کامل