Effect of a controlled sub-seabed release of CO2 on the biogeochemistry of shallow marine sediments, their pore waters, and the overlying water column

Lichtschlag, Anna ORCID: https://orcid.org/0000-0001-8281-2165; James, Rachael H.; Stahl, Henrik; Connelly, Douglas. 2015 Effect of a controlled sub-seabed release of CO2 on the biogeochemistry of shallow marine sediments, their pore waters, and the overlying water column. International Journal of Greenhouse Gas Control, 38. 80-92. 10.1016/j.ijggc.2014.10.008

Before downloading, please read NORA policies.

Preview

Text (Open Access paper)
1-s2.0-S1750583614003090-main.pdf - Published Version
Available under License Creative Commons Attribution.
Download (1MB) | Preview

Abstract/Summary

The potential for leakage of CO2 from a storage reservoir into the overlying marine sediments and into the water column and the impacts on benthic ecosystems are major challenges associated with carbon capture and storage (CCS) in subseafloor reservoirs. We have conducted a field-scale controlled CO2 release experiment in shallow, unconsolidated marine sediments, and documented the changes to the chemical composition of the sediments, their pore waters and overlying water column before, during and up to 1 year after the 37-day long CO2 release. Increased levels of dissolved inorganic carbon (DIC) were detected in the pore waters close to the sediment-seawater interface in sediments sampled closest to the subsurface injection point within 5 weeks of the start of the CO2 release. Highest DIC concentrations (28.8 mmol L−1, compared to background levels of 2.4 mmol L−1) were observed 6 days after the injection had stopped. The high DIC pore waters have high total alkalinity, and low δ13CDIC values (−20‰, compared to a background value of −2‰), due to the dissolution of the injected CO2 (δ13C = −26.6‰). The high DIC pore waters have enhanced concentrations of metals (including Ca, Fe, Mn) and dissolved silicon, relative to non-DIC enriched pore waters, indicating that dissolution of injected CO2 promotes dissolution of carbonate and silicate minerals. However, in this experiment, the pore water metal concentrations did not exceed levels considered to be harmful to the environment. The spatial extent of the impact of the injected CO2 in the sediments and pore waters was restricted to an area within 25 m of the injection point, and no impact was observed in the overlying water column. Concentrations of all pore water constituents returned to background values within 18 days after the CO2 injection was stopped.

Item Type:	Publication - Article
Digital Object Identifier (DOI):	10.1016/j.ijggc.2014.10.008
ISSN:	17505836
Additional Keywords:	Carbon capture and storage; CO2 leakage; Sediment biogeochemistry; Release of metals; Environmental impact
Date made live:	29 Oct 2014 10:19 +0 (UTC)
URI:	https://nora.nerc.ac.uk/id/eprint/508705

Item Type:

Publication - Article

Digital Object Identifier (DOI):

10.1016/j.ijggc.2014.10.008

ISSN:

17505836

Additional Keywords:

Carbon capture and storage; CO2 leakage; Sediment biogeochemistry; Release of metals; Environmental impact

Date made live:

29 Oct 2014 10:19 +0 (UTC)

URI:

https://nora.nerc.ac.uk/id/eprint/508705