Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.
Using data from recently completed hydrographic surveys of dissolvedinorganic carbon (DIC) and related tracers in the world's oceans,Sabine et al. (1) arrived at an estimate of 118 ± 19Pg C for the uptake of anthropogenic CO2 by the oceans through1994. This estimate uses the "C* method" pioneered by Gruber(2) and now widely applied to estimating ocean carbon changes.Here, I highlight several complications associated with theC* method that have not been previously discussed. Considerationof these factors suggests that estimates of ocean uptake ofanthropogenic CO2 may need revising.
One complication is that the ocean inventory of anthropogenicCO2 is an incomplete measure of the change in the ocean carboncontent. The term "anthropogenic CO2," as used by Sabine etal., refers to the excess carbon dioxide that has accumulatedin the ocean as a direct response to rising CO2 levels sincepreindustrial times. Changes in carbon accumulation driven byprocesses within the ocean, such as warming (whether anthropogenicor otherwise), or changes in ocean stratification are not countedas "anthropogenic" CO2. These contributions are certainly muchsmaller than the component driven by rising atmospheric CO2levels, but they are not necessarily negligible. A completeglobal carbon budget must therefore also include a term forthese ocean-driven exchanges of CO2.
It is relatively straightforward to estimate the direct effectof long-term warming on air-sea carbon exchanges (3, 4). Forexample, using the box-diffusion model (5) tuned for consistencyto match the Sabine et al. estimate of 118 petagrams of carbonin the absence of warming, the net uptake in the presence ofwarming is found to be 105 Pg C. This is consistent with a warmingcorrection of 13 Pg C (68). Warming releases CO2from the ocean primarily because CO2 is less soluble in warmerwater.
It is likely that warming over the past century has also influencedCO2 exchange indirectly through increases in the density stratificationof the upper ocean, thereby decreasing vertical mixing and increasingthe trapping of nutrients and metabolic CO2 in subsurface waters.There is no simple way to estimate this stratification effect,but based on the results of general circulation models (3, 4),the effect through 1994 is most likely on the order of +6 PgC, offsetting the warming effect. Combining the warming andstratification effects thus leads to an estimate of 7Pg C for the ocean-driven term, with an uncertainty that isnot well constrained but probably is about ±10 Pg C.
Another complication is that the ocean inventory of anthropogenicCO2 may not be determined reliably using the C* method in thepresence of warming or other ocean variability. The C* methodis a hybrid of two methods, the first applied in the upper oceanwhere the isopycnal layers are contaminated everywhere withanthropogenic CO2 and the second applied in the deeper waterswhere the isopycnal layers are partially uncontaminated. Inthe upper ocean, the C* method principally relies on chlorofluorocarbonventilation ages in combination with the known history of atmosphericCO2. If a different atmospheric history were used, the estimateof anthropogenic CO2 uptake in these water would change proportionally,which illustrates that the method is not a direct observationof carbon accumulation but effectively a model-dependent estimate,albeit a highly constrained one. This model assumes that theocean circulation has remained steady with time and is thereforesubject to error if circulation rates have changed. For example,the box-diffusion model indicates that if the vertical diffusionrates were 20% higher before 1980, the Sabine et al. estimate(1), which effectively projects modern diffusion rates overthe entire period, would underestimate the actual uptake by7 Pg C.
In the deeper waters, the C* method depends on the spatial gradientsin the tracer C*, which is a mathematical function of totalcarbon, oxygen, nitrate, phosphate, silica, alkalinity, temperature,and salinity. The assumption is made that the gradient in C*,along a given isopycnal surface from the older uncontaminatedwaters to the younger contaminated waters, is a measure of anthropogenicCO2. However, the gradient in C* can be produced not only byuptake of CO2 but also by other processes, particularly air-seaexchanges of heat and O2 (9). Based on the C* sensitivity toheat and O2 (10) and plausible estimates of changes in heatand O2 content of the deeper waters (1116), correctionson the order of 3 to 5 Pg C are implied, with the heat and O2effects partly canceling. More work is needed to assess thesecorrections as well as the impact on variable circulation, whichare complicated by our limited knowledge of global hydrographicchanges before the late 20th century. Until these correctionsare properly assessed, it seems appropriate to revise upwardthe uncertainty in the estimate of anthropogenic CO2 uptake.A reasonable revision might be from ±19 to ±23Pg C/year.
In summary, the Sabine et al. (1) estimate of anthropogenicCO2 uptake should be combined with an additional term of about7 ± 10 Pg C to account for air-sea CO2 exchangesdriven by warming and stratification. The error estimate onthe anthropogenic contribution should furthermore be increasedto about ±23 Pg C to reflect uncertainties associatedwith changes in ocean circulation, heat content, and O2 contenton the C* method. Combining these corrections yields an estimateof 111 ± 25 Pg C for the net oceanic uptake of CO2 from1800 to 1994. I hope that this comment will initiate a processto examine these corrections more closely.
Ralph F. Keeling
Scripps Institution of Oceanography La Jolla, CA 920930244, USA E-mail: rkeeling{at}ucsd.edu
2. N. Gruber, J. L. Sarmiento, T. F. Stocker, Global Biogeochem. Cycles10, 809 (1996). [CrossRef]
3. J. L. Sarmiento, T. M. C. Hughes, R. J. Stouffer, S. Manabe, Nature393, 245 (1998). [CrossRef]
4. G. K. Plattner, F. Joos, T. F. Stocker, O. Marchal, Tellus Ser. B Chem. Phys. Meteorol.53, 564 (2001).
5. H. Oeschger, U. Siegenthaler, U. Schotterer, A. Gugelmann, Tellus27, 168 (1975). [ISI]
6. This estimate is based on driving the box-diffusion model with the global average sea surface temperature (SST) from 1860 to 1994, as computed from the 5° by 5° global data set (7), and accounts for the effects of warming on CO2 solubility and carbon-system chemistry. The calculation neglects changes in temperature from 1800 to 1860, under the assumption that these changes were small (8).
7. P. D. Jones, A. Moberg, J. Clim.16, 206 (2003). [CrossRef]
9. C* is sensitive to air-sea O2 exchange despite the tendency for O2 to remain close to atmospheric equilibrium in surface waters. During photosynthesis in surface waters, for example, the tracer C* would be conserved were it not for air-sea exchange of CO2 and O2. These exchanges typically do not cancel because O2 equilibrates more rapidly than CO2. Rapid O2 equilibration thus actually drives changes in C*.
10. The specific sensitivity of C* to heat and O2 are 13 µmol kg1 °C1 and 0.8 mol mol1, as can be derived by formally differentiating the expression for C* with respect to O2 and potential temperature.
11. S. Levitus, J. I. Antonov, T. P. Boyer, C. Stephens, Science287, 2225 (2000).[Abstract/Free Full Text]
12. L. Bopp, C. Le Quéré, M. Heimann, A. C. Manning, P. Monfray, Global Biogeochem. Cycles16, 1022 (2002); 10.1029/2001GB001445. [CrossRef]
13. R. F. Keeling, H. Garcia, Proc. Natl. Acad. Sci. U.S.A.99, 7848 (2002).[Abstract/Free Full Text]
14. T. J. Crowley, S. K. Baum, K. Y. Kim, G. C. Hegerl, W. T. Hyde, Geophys. Res. Lett.30, 1932 (2003). [CrossRef]
15. R. J. Matear, A. C. Hirst, Global Biogeochem. Cycles17, 1125 (2003); 10.1029/2002GB001997. [CrossRef]
16. G. K. Plattner, F. Joos, T. F. Stocker, Global Biogeochem. Cycles16, 1096 (2002).
17. I thank R. Hamme and C. LeQuéré for valuable discussions. This work was completed, in part, while I was hosted at the Max Planck Institute for Biogeochemistry in Jena, Germany, and was supported by NSF grant ATM-0330096.
Received for publication 11 January 2005. Accepted for publication 16 May 2005.
The editors suggest the following Related Resources on Science sites:
In Science Magazine
TECHNICAL COMMENTS
Christopher Sabine and Nicolas Gruber (17 June 2005) Science308 (5729), 1743d.
[DOI: 10.1126/science.1109949] |Full Text »|PDF »
RESEARCH ARTICLES
Christopher L. Sabine, Richard A. Feely, Nicolas Gruber, Robert M. Key, Kitack Lee, John L. Bullister, Rik Wanninkhof, C. S. Wong, Douglas W. R. Wallace, Bronte Tilbrook, Frank J. Millero, Tsung-Hung Peng, Alexander Kozyr, Tsueno Ono, and Aida F. Rios (16 July 2004) Science305 (5682), 367.
[DOI: 10.1126/science.1097403] |Abstract »|Full Text »|PDF »|Supporting Online Material »
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
An estimate of anthropogenic CO2 inventory from decadal changes in oceanic carbon content.
T. Tanhua, A. Kortzinger, K. Friis, D. W. Waugh, and D. W. R. Wallace (2007)
PNAS
104, 3037-3042
|Abstract »|Full Text »|PDF »