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<br />moves westward and warms under the tropical sun (fig. 3.4 <br />of Brewer 1983). However, the tendency toward degassing <br />from seawater that is being warmed can be reversed by <br />rapid growth of plankton in nutrient-rich water. <br /> <br />Short-term exchanges of CO2 between the ocean and <br />the atmosphere are almost in balance, as figure 1 indicates. <br />The apparent net absorption by the ocean over the past few <br />decades has been driven by the rapid increase in the <br />atmospheric concentration, which either speeds CO2 <br />absorption or suppresses its escape depending on local <br />conditions. If the ocean warms as a result of global <br />climate change, its ability to absorb atmospheric CO2 will <br />be diminished slightly. Keeling et al. (1989) have <br />calculated that a slight observed warming of the sea surface <br />from 1978 to about 1988 reduced the total COz uptake over <br />the decade by roughly 3 Gt. <br />Short-term exchanges of CO2 between the ocean and <br />the overlying atmosphere involve only the ocean's mixed <br />layer. Convection and turbulence distribute dissolved CO2 <br />in its various forms rather uniformly throughout the mixed <br />layer in a few months. The depth of the mixed layer <br />varies, depending mainly on wind speed and vertical <br />density gradients, but averages around 75 m (Keeling et al. <br />1989). The mixed layer reaches its maximum depth in <br />areas where loss of heat from the sea surface to overlying <br />cold airmasses leads to convective overturning within it. <br />At high latitudes during winter, convective currents of <br />chilled surface water can penetrate downward as much as 1 <br />km, but mixing to that depth is incomplete. <br /> <br />2.3 Carbon in Seawater <br /> <br />In order to discuss CO2 in seawater quantitatively it <br />is necessary to consider the various forms that it assumes. <br />The CO2 dissolved in seawater is hydrated to form a weak <br />solution of carbonic acid (H2C03), which dissociates in two <br />stages to yield bicarbonate (HC03') and then carbonate <br />(C03 =) ions. The relative abundance of the various ions is <br />controlled by a number of buffering reactions, of which the <br />most important is <br /> <br />2 HC03' +- -+ H2C03 + C03 = <br /> <br />The equilibrium constants for the various reactions <br />vary with temperature and the pH value (acidity). <br />According to a review by Archer (1990), only 1 percent of <br />the carbon in seawater remains as CO2 or undissociated <br />H2C03, 88 percent of it exists as bicarbonate ions, and the <br />other 11 percent as carbonate ions. Some writers use the <br />expression "total CO2'' to mean the total of dissolved CO2 <br />gas, H2C03, and bicarbonate and carbonate ions. <br /> <br />The fact that CO2 forms H2C03, which then <br />dissociates, makes it possible for seawater to hold about 30 <br />times more CO2 under present conditions than it could <br />otherwise. Although oxygen is about 600 times as plentiful <br />as CO2 in the atmosphere, it is only about 20 times as <br />plentiful in the ocean as the CO2 equivalent of the carbon <br />in the ocean. However, there is resistance to further <br />additions of CO2 to seawater. This resistance is expressed <br />as a buffer factor, which is sometimes called the Revelle <br />factor (Brewer 1983). The Revelle factor is a function of <br />temperature, alkalinity and salinity, and so varies from <br /> <br />place to place. Its present values are around 10, which <br />means that changes in the total concentration of carbon in <br />seawater, expressed as a percentage of the existing <br />concentration, are only 0.1 times the corresponding <br />changes in the partial pressure of CO2 gas in the overlying <br />atmosphere (Brewer 1983). Even so, seawater still is <br />taking up about 3 times more CO2 than it would if CO2 did <br />not dissociate. <br /> <br />Numbers quoted in table 8 of Keeling et al. (1989) <br />can be combined to show that the ocean's mixed layer now <br />holds roughly the same amount of carbon as does the <br />atmosphere. Using that result and the current Revelle <br />factor of 10, one can estimate the final apportionment <br />between the atmosphere and the mixed layer of incremental <br />amounts of atmospheric CO2, As an increase of 10 percent <br />in the atmospheric concentration of CO2 will produce only <br />a 1 percent increase in the total carbon content of the <br />mixed layer, equilibrium is reached once the mixed layer <br />takes up 0.09 Gt of each additional gigaton of carbon, <br />leaving the remaining 0.91 Gt in the atmosphere. <br /> <br />2.4 Intermediate Cycles: Carbon in the Deep Ocean <br /> <br />It has been estimated that the CO2 released from <br />fossil fuels since the beginning of the Industrial Revolution <br />has been divided about equally between the ocean and the <br />atmosphere; yet the result just quoted in section 2.3 shows <br />that the mixed layer can not absorb and hold more than <br />one-tenth of the excess carbon being released to the <br />atmosphere each year. The mixed layer's ability to <br />continue to draw down atmospheric CO2 depends on <br />exchanges with the deep ocean, which holds about 98 <br />percent of the carbon listed for the oceanic reservoir in <br />table 1. Exchanges of carbon between the mixed layer and <br />the ocean depths are brought about by ocean currents, <br />large-scale turbulence and biological processes. <br /> <br />(1) <br /> <br />All of the oceans share a common circulation. It is <br />characterized by regions where cold water sinks into the <br />depths, especially in the Weddell Sea near Antarctica and <br />between Greenland and Norway in the North Atlantic, and <br />by regions where cold water from the depths reappears at <br />the surface. Upwelling is marked along the west coast of <br />South America, for example. The deep-ocean circulation <br />proceeds very slowly, with complete circuits taking <br />hundreds or thousands of years. Tritium released by <br />nuclear bomb testing in 1962 and carried downward in the <br />North Atlantic circulation still had not penetrated south of <br />300 N in the deep Atlantic by 1981 (Brewer 1983). <br /> <br />The cold water that sinks into the OCf<'Ul depths <br />tends to be rich in CO2 and associated forms of carbon <br />simply because it is cold. Its carbon content is enhanced <br />further by biological processes. Organisms growing in the <br />mixed layer deplete its CO2 significantly, thereby making <br />possible the uptake of more atmospheric CO2. and ensuring <br />that the sinking water carries significant amounts of carbon <br />downward in organic as well as inorganic forms. On its <br />long circuit in the deep ocean, the water is further enriched <br />by organic waste falling from the mixed layer. <br />Decomposition of this waste gives off CO2, which leads to <br />an increase of some 10 percent in the concentration of CO2 <br />and associated ions over the first kilometer downward from <br /> <br />108 <br />