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| JOURNAL HOME | HELP | CONTACT PUBLISHER | SUBSCRIBE | ARCHIVE | SEARCH | TABLE OF CONTENTS |
1 Department of Civil and Environmental Engineering
Massachusetts Institute
of Technology, Room 48-216b
Cambridge, MA 02139, USA
E-mail:
eeadams{at}mit.edu
2 Department of Global Ecology, Carnegie Institution
Stanford University, 260
Panama St., Stanford, CA 94305, USA
E-mail:
kcaldeira{at}stanford.edu
| ABSTRACT |
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KEYWORDS: ocean carbon sequestration, CO2 ocean storage, environmental impact, climate change
| INTRODUCTION |
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Over the past 200 years, oceans have taken up over 500 Gt of CO2
from the atmosphere, compared with over 1300 Gt CO2 emitted to the
atmosphere (IPCC 2005). As a
result, the pH of the surface ocean (the upper few hundred meters that are in
greatest contact with the atmosphere) has dropped by about 0.1 pH units from
the preindustrial value of about 8.2. This causes concern for the health of
coral reefs and other organisms that use calcium carbonate in their skeletons
or shells. FIGURE 2
presents model results for ocean pH if known fossil fuel reserves are burned
and CO2 is released. The atmospheric concentration would increase
to
2000 ppm in 300 years (similar to
FIGURE 1), and ocean
surface pH would drop by more than 0.7 units
(Caldeira and Wickett 2003). By
injecting some of the CO2 into the deep ocean, the time until it
disperses to surface water is extended, allowing the change in pH to be
distributed more uniformly with depth.
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| CAPACITY |
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CO2 exists in seawater in various forms as part of the carbonate
system:
![]() | (Eq.1) |
The relative proportions of these species are defined by the pH of the
solution and by equilibrium relationships. Dissolving additional
CO2 increases production of hydrogen ions (decreasing pH), but the
change is buffered by conversion of carbonate into bicarbonate. Thus, the
principal reactions for CO2 dissolution in seawater are as follows:
![]() | (Eq.2) |
![]() | (Eq.3) |
Decreased pH is one of the principal environmental impacts threatening marine organisms; the other is the concentration of CO2 itself. Near the injection point, changes in pH and CO2 concentration would be greatest, so injection schemes would have lowest impact if dilution is maximized. Far from the injection point, as CO2 becomes widely distributed in the ocean, its impact would be similar to that of anthropogenic CO2 absorbed from the atmosphere. Adding about 2000 Gt CO2 to the ocean would reduce the average ocean pH by about 0.1 units, similar to the change already observed in the surface ocean. Adding about 5600 Gt CO2 (about 200 years of current emissions) would decrease the average ocean pH by about 0.3 units (IPCC 2005).
The impact of such changes is not well known. However, one can examine spatial and temporal variations in ocean pH to understand how much change might be tolerated. The pH variability within latitudinal bands in each of the three major oceans (Pacific, Atlantic, Indian) during the 1990s was roughly 0.1 unit (IPCC 2005). If a change of 0.1 unit is assumed as a threshold tolerance and if the CO2 is stored in the bottom half of the ocean (to maximize retention), approximately 1000 Gt CO2 could be stored, enough to stabilize atmospheric concentrations at 500 ppm over the next 50 years, assuming energy consumption follows current trends and no other mitigation measures are put into place (Pacala and Socolow 2004). It should be realized that over the long term (millennia), the change in whole-ocean pH would ultimately be the same, whether CO2 is released into the atmosphere or injected into the deep ocean, because thermodynamics drives the system to equilibrium. However, in the shorter term (several centuries), injecting into the deep ocean, below 1000 m depth, would limit pH drop in the near-surface, where marine biota are most plentiful, thus decreasing the adverse impact in the surface ocean.
| INJECTION METHODS |
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5.75), is a solid in
which each CO2 molecule sits in a cage-like structure of water
molecules held together by hydrogen bonds. Unlike methane hydrates, which have
a similar structure but are positively buoyant
(Ruppel 2007), pure
CO2 hydrates are about 10% denser than seawater. Unless the
surrounding water is saturated with CO2, the hydrate is unstable,
but it dissolves more slowly into seawater than does liquid
CO2.
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Another dissolution option is to inject liquid CO2 into a vessel where it can react at a controlled rate with seawater to form hydrates. While 100% reaction efficiency is difficult to achieve, laboratory and field experiments indicate that CO2 sinks with as little as about 15-25% reaction efficiency (Tsouris et al. 2007). Instability leads to dissolution and dispersion during descent. The hydrate reactor could be towed from a moving ship, promoting additional dilution, or attached to a fixed platform, where the large concentration of dense particles and the increased seawater density caused by hydrate dissolution would create a sinking plume (Wannamaker and Adams 2006).
Dissolving high concentrations of CO2 into seawater and then releasing the solution at the seafloor is another option (Haugan and Drange 1992). Enrichment with CO2 causes only a slight density increase, but it is sufficient to promote sinking, especially within a submarine canyon. The environmental impact is higher, because the plume is more concentrated and it would come into direct contact with the seafloor, home to an abundance of relatively immobile fauna, bacteria, and algae. Alternatively, creating a CO2 lake on the seafloor minimizes leakage to the atmosphere and exposure to biota (Ohsumi 1995; Haugan and Alendal 2005). A CO2 lake would exist partly in the form of solid hydrates, which would slow dispersion to the water column, increasing retention time. Producing a lake would require more advanced technology and perhaps cost more than other options, because the lake must be more than 3000 m below the water surface.
Retention could be increased further using the reaction of CO2 with carbonate minerals. Anthropogenic CO2 currently transported to the deep ocean will equilibrate with carbonate sediments over a period of about 6000 years (Archer et al. 1998). Technical means could be used to accelerate this reaction, increasing effectiveness and diminishing the environmental impact. Power plant gas could be dissolved in seawater (Eq. 2) and then reacted with crushed limestone, either at the power plant or at the point of release, thus buffering pH change (Caldeira and Rau 2000). Conversely, an emulsion of liquid CO2 and water could be stabilized by fine particles of pulverized limestone; the emulsion would be sufficiently dense to sink, and pH would be partially buffered by the limestone (Golomb et al. 2007). Drawbacks to these approaches include the cost to mine, crush, and transport large quantities of carbonate rock.
| EFFECTIVENESS |
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As a result of anthropogenic input, the atmosphere and ocean are currently
out of equilibrium, so most emitted CO2 will ultimately end up in
the ocean. The percentage of CO2 permanently sequestered is defined
by thermodynamics and depends on the atmospheric concentration
(TABLE 1). At
today's atmospheric level of
380 ppm, nearly 80% of CO2
emitted either to the atmosphere or to the ocean would
become permanently stored in the ocean, while at a concentration of 750 ppm,
70% would be stored. Of course, even at equilibrium, CO2 would
continue to be exchanged between the atmosphere and the ocean, so the carbon
in the ocean on any given day would not be exactly the same carbon present on
the previous day, even though the total would be constant. The predictions in
TABLE 1 include the
possibility of increased carbon storage in the terrestrial biosphere, but do
not consider natural or engineered dissolution of carbonate minerals. Over
thousands of years, retention would increase somewhat as CO2 reacts
with ocean sediments.
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TABLE 1 implies that, for CO2 injected into the ocean today, the net quantity stored ranges from 100% (now) to about 70-80% as the atmosphere approaches equilibrium with the ocean. One can also define retention as the fraction of injected CO2 that is retained without ever reaching the surface; this fraction ranges from 100% at the time of injection to zero at equilibrium. The exact time depends on the location and depth of the injection.
Several computer-modeling studies have investigated CO2 retention time in the world's oceans. The most comprehensive summary is the Global Ocean Storage of Anthropogenic Carbon (GOSAC) intercomparison study of several ocean general circulation models (OGCM). Ten models simulated the fate over 500 years of CO2 injected at seven locations and three depths (Orr 2004). FIGURE 5 shows the fraction of CO2 retained as a function of time, averaged over the seven sites. Although there is substantial variability, all models indicate increased retention with injection depth, and most predict over 70% retention after 500 years for injection at 3000 m. Note that these calculations assume CO2 is dispersed in the water column at the injection depth. Formation of a CO2 lake or reaction with marine sediments could increase retention time.
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| LOCAL ENVIRONMENTAL IMPACT AND PUBLIC PERCEPTION |
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A number of studies have summarized the potential impact on a variety of organisms, including adult and developing fish, zooplankton, and benthic fauna (Kikkawa et al. 2003; Ishimatsu et al. 2004; Pörtner et al. 2004; Watanabe et al. 2006). Earlier studies focused on the lethal impact on coastal fauna exposed to strong acids such as HCl (Auerbach et al. 1997), but recent work has examined the impact on deep-water organisms when exposed to CO2, including sublethal effects (Kurihara et al. 2004). Organisms experience respiratory stress (decreased pH limits oxygen binding and transport of respiratory proteins), acidosis (low pH disrupts acid/base balance), and metabolic depression (elevated CO2 causes some animals to reach a state of torpor). Data show a number of trends: (1) H2CO3 generally causes greater stress on an organism than an equivalent change in pH produced by another acid; (2) there are large differences in tolerance among different species and among different life stages of the same species; and (3) the duration of stress, as well as the level of stress, are important. While some studies suggest that deep organisms would be less tolerant than surface organisms, other studies have shown the opposite. Likewise, some animals are able to avoid regions of high CO2 concentration (Vetter and Smith 2005), while others are less able (Tamburri et al. 2000). Results generally imply that lethal effects can be avoided by achieving high near-field dilution. However, more research is needed, especially at the community level (e.g. studies of reduced lifespan, reproduction effects, and tolerance to other stresses).
The viability of ocean storage as a greenhouse gas mitigation option hinges on social, political, and regulatory considerations. In view of public precaution toward the ocean, which is a common, global resource, the strategy will require that all parties (private, public, non-governmental organizations) be included in ongoing research and debate. But the difficulty in this approach is highlighted by the recent experience of an international research team whose aim was to assess ocean carbon sequestration, as encouraged by the United Nations Framework Convention on Climate Change. A major part of their activity would have been a field test with 5 tons of CO2 released off the coast of Norway. The plan was to monitor the physical, chemical, and biological effects of the injected CO2 over a period of about a week. However, lobbying from environmental groups caused the Norwegian minister of the environment to rescind the group's permit (Giles 2002). Such actions unfortunately prevent collection of data that are critical for policy makers to evaluate the prudence of full-scale implementation.
| COSTS AND COMPARISON WITH OTHER STORAGE METHODS |
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The aim of geological sequestration is to permanently trap the CO2 within well-defined regions, so that it cannot interact with terrestrial or oceanic ecosystems. Sometimes CO2 can be used to enhance oil recovery or coalbed methane production. For these reasons, geological storage has been favored. In contrast, most ocean disposal schemes aim to minimize impact by diluting the CO2 in the vastness of the ocean, and while it may be isolated from the atmosphere for centuries, approximately 20-30% of it will eventually leak back. The ocean storage option that promises the most permanence is mineral carbonation, but this is more expensive—IPCC (2005) estimates the cost at US$50-100 per ton CO2. On the other hand, compared with deep underground storage, CO2 dispersed in the ocean is relatively easy to monitor, and because it is dispersed, the CO2 that eventually reaches the atmosphere will escape slowly.
In a method that is hybrid between ocean and geologic storage, CO2 would be injected into marine sediments, deep offshore (House et al. 2006). Because of the relatively high pressure and low temperature in this environment, the CO2 would be negatively buoyant, perhaps forming solid hydrates, thus minimizing leakage through the sediment-water interface. And any CO2 that was eventually released to the ocean would be dispersed and diluted.
Another form of ocean sequestration is enhanced production of biomass. Fertilizing portions of the world's oceans with iron would stimulate phytoplankton growth. The phytoplankton would increase the rate of biological uptake of CO2 from the surface water and the atmosphere, and a portion would be transported to the ocean depths when the plankton dies. Iron fertilization is relatively inexpensive, and the organisms do most of the capture and transport, making this process an attractive solution. However, the technique is considered risky because it relies on deliberate manipulation of an ecosystem, with uncertain effects. At least ten international field experiments have been conducted to examine the short-term effects of iron fertilization (Coale et al. 2004). Although these experiments have demonstrated a clear response over the short term, the long-term effectiveness and the potential for detrimental changes to marine ecosystems are uncertain.
| CONCLUSIONS |
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| JOURNAL HOME | HELP | CONTACT PUBLISHER | SUBSCRIBE | ARCHIVE | SEARCH | TABLE OF CONTENTS |