TERRAPUB Journal of Oceanography

Journal of Oceanography, Vol. 60 (No. 4), pp. 751-758, 2004

Small Scale Field Study of an Ocean CO2 Plume

Peter G. Brewer1*, Edward Peltzer1, Izuo Aya2, Peter Haugan3, Richard Bellerby3, Kenji Yamane2, Ryuji Kojima2, Peter Walz1 and Yasuharu Nakajima4

1Monterey Bay Aquarium Research Institute, Moss Landing, CA 95039, U.S.A.
2Osaka Branch, National Maritime Research Institute, Osaka 576-0034, Japan
3Geophysical Institute, University of Bergen, N-0057 Bergen, Norway
4National Maritime Research Institute, Tokyo 181-0004, Japan

(Received 29 September 2003; in revised form 19 April 2004; accepted 20 April 2004)

Abstract: We have carried out a small-scale (~20 l) CO2 sequestration experiment off northern California (684 m depth, ~5°C, background ocean pH ~7.7) designed as an initial investigation of the effects of physical forcing of the fluid, and the problem of sensing the formation of a low pH plume. The buoyant CO2 was contained in a square frame 1.2 m high, exposing 0.21 m2 to ocean flow. Two pH electrodes attached to the frame recorded the signal; a second frame placed 1.9 m south of the CO2 pool was also equipped with two recording pH electrodes. An additional pH electrode was held in the ROV robotic arm to probe the fluid interface. Local water velocities of up to 40 cm sec-1 were encountered, creating significant eddies within the CO2 box, and forcing wavelets at the fluid interface. This resulted in rapid CO2 dissolution, with all CO2 being depleted in a little more than 2 days. The pH record from the sensor closest (~10 cm) to the CO2 showed many spikes of low pH water, the extreme value being ~5.9. The sensor 1 m immediately below this showed no detectable response. The electrodes placed 1.9 m distant from the source also recorded very small perturbations. The results provide important clues for the design of future experiments for CO2 disposal and biogeochemical impact studies. These include the need for dealing with the slow CO2 hydration kinetics, better understanding of the fluid dynamics of the CO2-water interface, and non-point source release designs to provide more constant, controlled local CO2 enrichments within the experimental area.

*Corresponding author E-mail: brpe@mbari.org

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