As the burning of fossil fuels in the last century raised atmospheric carbon dioxide levels, was the ocean a source or a sink for CO2or both? A comprehensive survey of CO2 in the world's oceans may give scientists the chance to find out.
By Christopher L. Sabine, Princeton University; Douglas W. R. Wallace, Brookhaven National Laboratory, Upton, N.Y.; and Frank J. Millero, University of Miami, Miami, Fla.
Industrial emissions of carbon dioxide (CO2, the chief greenhouse gas), have more than tripled in the past 40 years, causing concern that increased heat-trapping gas in the atmosphere could cause global warming. Predicting long-term climate trends is tricky, particularly if the capacity of the ocean to take up or give off CO2 is unknown. Estimates based on model results suggest that the oceans could remove approximately 37% of the CO2 produced each year from the burning of fossil fuels, but to date, scientists have not been able to confirm this number with direct oceanographic measurements. It is important to know how much CO2 the oceans are taking up because they may help to reduce the amount of warming caused by the greenhouse effect.
In 1979, a paper published in Science pointed out that model estimates of CO2 uptake could only be confirmed with oceanic CO2 measurements made at accuracy levels that were not technologically possible at that time.
Seventeen years later, the technology has improved, and a global survey of CO2 is nearly complete. Enough high
quality data have finally been gathered to determine the distribution and mass of January 1996 marked the completion of one ambitious part of the global oceanic inorganic carbon survey: a 14-month, 92,000-km-long research cruise in the Indian Ocean.
This survey, conducted with the international World Ocean Circulation Experiment- Hydrographic Program (WOCE-HP), is part of a project involving 10 U.S.
universities and national laboratories
that have been working together since 1990 to acquire a high-quality inorganic carbon data set for all of the world's oceans.
Why are so many accurate carbon measurements in the oceans needed?
The CO2 measurements must be highly accurate because scientists are trying to quantify a very small change in a very big number. Compared to the tremendous amount of carbon naturally stored in the ocean, the increase in CO2 from human activities is very small.
Approximately 98.5% of the CO2 in the ocean-atmosphere inventory is
found in the ocean. The oceans hold most of the carbon because CO2 is approximately 30 times more soluble in water than other common gases.
CO2 molecules also react with water in the ocean to form carbonic acid and its dissociation products: carbonate and bicarbonate ions.
Because the oceans naturally contain much more carbon than the atmosphere, a dramatic industry-generated increase in CO2 concentrationsuch as that observed in the atmosphereis not seen in the oceans.
The anticipated total CO2 (TCO2) increase in surface water is approximately 0.05% per yearonly one-tenth of the increase observed in the atmosphere.
Detecting a signal that small, given the complicated carbon chemistry in the ocean, requires extremely accurate measurements.
 The figures illustrate the horizontal and vertical changes in oceanic CO2 levels observed in the Indian Ocean.
Fluctuations in these CO2 levels in the upper ocean can be 10 to 100 times more than the annual anthropogenic increase. Therefore researchers have to make hundreds of thousands of CO2 measurements to accurately distinguish the natural variability from the CO2 increase due to rising atmospheric concentrations.
Fig. 1. Maps of a) the distribution of total CO2 and b) the distribution of total alkalinity on a constant density surface ([theta-sigma] = 27.5; depth range 11001400 m) in the Indian Ocean.
There were 1244 stations occupied as part of the WOCE Indian Ocean Survey (locations identified with black dots on the map)10 times the number of Geochemical Ocean Sections Survey sampling sites 18 years earlier.
Uptake of carbon in the surface water by marine organisms for photosynthesis and the subsequent remineralization of the organic matter at depth after the organisms die strongly influence the distribution of carbon in the oceans.
The fact that CO2 is more soluble in cold, polar water than in warm water also influences the distribution. These two processes, (termed the biological and solubility pumps), and the relatively slow mixing time of the oceans, result in large horizontal and vertical variations of CO2 in the oceans.
(see figures)
The maps along the [theta-sigma] = 27.5 density surface in the figure show that both the TCO2 and total alkalinity (TA) concentrations increase from south to north in the Indian Ocean.
The net water flow along this surface is from south to north, so the northern waters have had more time to accumulate carbon from the remineralization of organisms sinking from the surface.
The concentrations of both TCO2 and TA are generally higher in the eastern basin than at the same latitude in the west, reflecting the contribution of relatively low-carbon Atlantic water from around the southern tip of Africa.
The highest CO2 concentrations are observed in the deep waters at the northern end of both sections (see figure).
The lowest concentrations occur in northern surface waters where the biological pump
removes carbon. Beyond these similarities, the TCO2 and TA distributions in the upper waters are very different. For example, the Antarctic Intermediate Water can be observed as a
TA minimum where it leaves the surface at approximately 50°S (the blue-green tongue between the yellow regions), but it is not readily apparent in the TCO2 section.
The difference in the vertical gradients of TCO2 and TA shows that each of the carbon parameters is influenced differently by the various processes.
For example, TCO2 is influenced by photosynthesis and remineralization to a much greater degree than TA. The constant rain of organic matter from the surface waters and subsequent remineralization maintain the sharp
increase in TCO2 with depth that masks the Antarctic Intermediate Water signal. By comparing and contrasting the distributions of the different carbon parameters, the processes that transport carbon within the ocean can be evaluatedan important first step in estimating the mass of anthropogenic CO2 stored in the ocean
Three approaches, which were limited in the past due to both the quantity and quality of the available data, are now being employed with the survey data to quantify the oceanic sink for anthropogenic CO2.
The first approach uses measurements of the difference in the sea and air CO2 levels together with wind speed observations to
calculate the flux of CO2 across the sea-air interface. Scientists can determine how much CO2 is entering the ocean by summing up this flux over the entire ocean.
This approach is the most direct way to estimate the oceanic CO2 uptake, but it is severely limited by spatial and temporal variability in the oceans.
By combining recently obtained measurements of pCO2 (partial pressure of CO2 gas) with the existing data set, these uncertainties can be reduced.
The differences of pCO2 in ocean water and in air along the cruise tracks in the Indian Ocean demonstrate the wide spatial differences that cause the ocean to be a sink or a source of CO2, depending upon the location and conditions (see figure).
Positive values indicate that CO2 is moving from the ocean to the atmosphere, and negative values indicate that the oceans are taking up CO2.
The high sea water CO2 concentrations relative to the atmosphere in the Arabian Sea region (red, yellow, and green) indicate that this area was a potential significant source of CO2 to the atmosphere in the summer of 1995, while the southwestern Indian Ocean was a sink for CO2 at the time of sampling.
Fig. 2. Map of surface [Delta]pCO2 (sea-air)
The high seawater values in the Arabian Sea were caused by the upwelling of CO2-rich waters associated with the southwest monsoon, a natural phenomenon with strong seasonality.
This example indicates why we need to understand naturally occurring variations before quantifying the anthropogenic contributions.
A second approach is to evaluate the increase in carbon in the interior of the ocean due to the invasion of anthropogenic CO2.
One "time-series" method uses measurements of TCO2 made at a certain time to develop a predictive equation based on the relationship between the observed TCO2 and salinity, temperature, oxygen and total alkalinity (or silicate), which are measured at the same time.
These relationships hold over large spatial scales,
and their use drastically reduces the complicating effects of natural variability in surface waters by examining the signal in the more stable, deeper waters.
The difference between TCO2 measurements made at different times (for example over decades) will isolate the anthropogenic contribution.
Systematic changes in the difference between the predicted and measured TCO2 concentrations over time provide a direct estimate of oceanic CO2 flux caused by the uptake of anthropogenic CO2.
This technique was applied to the recently collected WOCE Indian Ocean survey data set and data from the 19771978 Geochemical Ocean Sections Survey (GEOSECS) of the Indian Ocean.
The difference between the measured and predicted TCO2 concentrations for the same area of the Indian Ocean examined 18 years apart is consistent with the anthropogenic CO2 uptake anticipated to be ~1 µmol kg-1 yr-1 for the 18 years since GEOSECS.
Another method of estimating the anthropogenic CO2 inventory uses the difference ([Delta]C*) between the WOCE Indian Ocean TCO2 concentrations (corrected for the influence of the biological pump) and the TCO2
concentration these waters would have had when they were formed at the surface assuming a preindustrial atmospheric CO2 concentration of 280 µatm.
Since the deep waters (2000 m) actually were formed before anthropogenic CO2 was added to the atmosphere, they provide a baseline for the calculations.
The difference between [Delta]C* in deep (2000 m) water and in shallower waters can be interpreted as the anthropogenic inventory. This inventory is larger than the "time-series" inventory because it integrates changes since preindustrial time, not just since the last 18 years.
These assessments imply that approximately 28% of the total anthropogenic CO2 inventory in this area of the Indian Ocean has accumulated in the last 18 years.
The distribution of CO2 between sea and air has changed dramatically during glacial and interglacial climate changes.
A critical issue in predicting future atmospheric CO2 levels, and in developing policies designed to control CO2 increases in the future, is how the oceanic uptake might change as atmospheric CO2 levels continue to increase and if the climate changes.
Direct measurements help to determine the current or past oceanic responses to anthropogenic CO2. To predict how the oceans will respond in the future, however, requires the use of three-dimensional global carbon models.
An important test of how these models perform lies in how well they can reproduce current ocean carbon distributions and transports.
The global CO2 survey is finally providing the comprehensive data set necessary for this model validation.
The cooperative research of numerous scientists has generated a quantity and quality of data far greater than previously achieved.
Data from the current global survey are being made available on a cruise by cruise basis. As these data become finalized, they will be archived and made available to the public with an array of past carbon work at the Carbon Dioxide Information Analysis Center at the Oak Ridge National Laboratory.
The only major region that remains to be sampled is the North Atlantic Ocean, which was last sampled extensively during 19811983. The resulting data set will be a resource used for decades by scientists investigating regional and global-scale carbon cycle problems and those involved in making decisions about energy policy and future climate.
For more information on the Global CO2 survey and the availability of carbon data, refer to the World Wide Web site: http://cdiac.esd.ornl.gov/cdiac/oceans/home.html.
Source: Eos, February 4, 1997, p. 49.
As a member of the geosciences research staff at Princeton University, Christopher Sabine travels around the world on research ships making inorganic carbon measurements to better understand the role of the oceans in the global cycling of carbon dioxide.
Sabine's interest in oceanography began as a young teenager when his parents sold their house and the family spent a year sailing around the Bahamas on a 44-foot sailboat.
"The ocean is a complex and fascinating environment surrounded by a lot of mystery and myth," Sabine said."I simply wanted to understand it better."
After returning to the states and finishing high school in Charleston, South Carolina,
Sabine earned a bachelor of science degree in marine science at Texas A&M University at Galveston and a Ph.D. in oceanography at the University of Hawaii.
Sabine took a postdoctoral position at Princeton in 1992 and established the carbon measurement division of the ocean tracers laboratory. Most of his research is funded by the federal government.
The Department of Energy, for example, provided much of the funding for the global CO2 survey to help determine how they should regulate the tremendous amount of carbon dioxide released from the burning of fossil fuels by power plants and automobiles.
His advice to students interested in science is to find someone working in the particular field that you are interested in and see what they really do, day-in and day-out.
Being a scientist can be very rewarding work, but it can also be very mundane, difficult and frustrating, said Sabine. If you decide you want to become a scientist, he noted, concentrate on the basics of math and science and stay focused on your dream.
If you like the oceans, remember that oceanographic research encompasses chemistry, geology and physics, as well as biology. There is much more to oceanography than simply studying whales and dolphins.
A Small Change in a Big Number
Global Variations in Oceanic CO2
Techniques for Studying Anthropogenic CO2 in the Ocean
GLOSSARY
A Few Words About Author Christopher Sabine ...
Back to Science for Everyone