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PNNL-13501 - Pacific Northwest National Laboratory

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Environmental Fate and Effects of Deep Ocean Carbon Sequestration<br />

Study Control Number: PN00041/1448<br />

Ann Drum Skillman, Michael Huesemann, Eric Crecelius<br />

The emission of man-made sources of CO2 into the atmosphere is considered a major factor in the greenhouse effect<br />

leading to global warming. Several options for capturing and sequestering this CO2 have been proposed. These options<br />

include deep-ocean injection. This study examined the effects of CO2 ocean sequestration on marine nitrification<br />

processes and associated environmental impacts.<br />

Project Description<br />

In an attempt to slow down global warming, it has been<br />

proposed to reduce the rise of atmospheric carbon dioxide<br />

concentrations by disposing CO2 (from the flue gases of<br />

fossil fuel fired power plants) into the ocean. The release<br />

of large amounts of CO2 into mid or deep ocean waters<br />

will result in large plumes of acidified seawater with pH<br />

values ranging from 6 to 8. To determine whether these<br />

CO2-induced pH changes have any negative effect on<br />

marine nitrification processes, surficial (euphotic zone)<br />

and deep (aphotic zone) seawater samples were sparged<br />

with CO2 for varying time durations to achieve a specified<br />

pH reduction and the rate of microbial ammonia oxidation<br />

was measured spectrophotometrically as a function of pH.<br />

For both seawater samples taken from either the euphotic<br />

or aphotic zone, the nitrification rates dropped drastically<br />

with decreasing pH. Relative to nitrification rates in the<br />

original seawater at pH 8, nitrification rates are reduced<br />

by about 50% at pH 7 and by more than 90% at pH 6.5.<br />

Nitrification is essentially completely inhibited at pH 6.<br />

Introduction<br />

The combustion of fossil fuels during the last two<br />

centuries has significantly increased the concentration of<br />

carbon dioxide in the atmosphere and this is predicted to<br />

result in global warming and a wide range of concomitant<br />

negative environmental and social impacts (Houghton<br />

1997; Rayner and Malone 1998). To reduce the future<br />

potential impacts of global warming, carbon dioxide<br />

could potentially be removed from either the atmosphere<br />

or from the flue gases of power plants by sequestering it<br />

in terrestrial ecosystems, geological formations, or<br />

oceans. A number of different ocean disposal strategies<br />

have been proposed including the release of CO2 enriched<br />

seawater at 500 to 1000 m depth, or the injection of liquid<br />

CO2 at 1000 to 1500 m depth. The CO2 injections will<br />

result in large pH plumes around the injection points<br />

(Figure 1) (DOE 1999; Caulfield et al. 1997; Herzog et al.<br />

1996). Modeling results indicate that the pH around the<br />

218 FY 2000 <strong>Laboratory</strong> Directed Research and Development Annual Report<br />

injection point could be less than 5.8 and the steady-state<br />

plume of seawater with a pH less than 6.6 could be at<br />

least 25 km long and 1000 m wide and after a 20-year<br />

continuous CO2 injection could be more than 1000 miles<br />

long (DOE 1999; Caulfield et al. 1997; Herzog et al.<br />

1996).<br />

Figure 1. Conceptual diagram of several methods of ocean<br />

sequestration of CO 2<br />

Little is known about the potential environmental effects<br />

of CO2 disposal in oceans including impacts to the marine<br />

nitrogen cycle. Figure 2 shows a conceptual model of the<br />

oceanic nitrogen cycle (Libes 1992). Most of the nitrogen<br />

from phytoplankton growing in the euphotic zone is<br />

recycled by bacteria and zooplankton while the remaining<br />

nitrogen sinks as particulate organic material into the<br />

aphotic zone. While slowly sinking toward the ocean<br />

floor, aerobic bacteria first convert the particulate organic<br />

nitrogen into dissolved organic nitrogen and subsequently<br />

cause the release of free ammonium into the seawater.<br />

Ammonium is readily oxidized to nitrite and then to<br />

nitrate in a stepwise process called nitrification. The<br />

resulting nitrate accumulates in the deep ocean but is<br />

eventually up-welled back into the euphotic zone where it<br />

serves as new nitrogen for the growth of phytoplankton.<br />

The import of new nitrogen from the aphotic zone is very<br />

substantial and serves as an important nutrient source for<br />

oceanic primary productivity and world fisheries (Libes<br />

1992; Capone 2000; Falkowski et al. 1998).

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