Background Information

A dramatic increase in the atmospheric concentration of carbon dioxide (CO2) has been directly observed over the past 30 years (Keeling et al. 1989). Although the present growth rate of CO2 in the atmosphere is about 3.4 gigatons (1015 g) of carbon per year (GtC/yr), the present estimate of anthropogenic CO2 sources to the atmosphere is much larger [approximately 6 GtC/yr (IPCC 1990)]. Most of the CO2 (77%) released to the atmosphere originates from the combustion of fossil fuels (Marland and Rotty 1984). The remainder is estimated to originate from deforestation and changing land use patterns (IPCC 1990). Since the growth rate of CO2 in the atmosphere is less than the rate of carbon release, some of the anthropogenic carbon released to the atmosphere must be absorbed by either the terrestrial biosphere or the oceans.

The oceans have been suggested as a repository for carbon dioxide from the atmosphere through a chemical and biological pathway. Carbon dioxide dissolves readily in the surface oceans. The dissolved gas reacts with water to form carbonic acid which rapidly dissociates to bicarbonate and carbonate ions. Ocean plants can also draw down CO2 , some of which is converted to particulate matter which sinks out of surface waters.

The uncertain role of the ocean in absorbing anthropogenic carbon from the atmosphere has stimulated interest in the cycling and fate of carbon in the sea. The Pacific Marine Environmental Laboratory (PMEL) made measurements on 5 cruises (12 legs) in the Pacific and Indian Oceans (Fig. 1) to determine the concentrations of trace gases in the atmosphere and in surface seawater. These cruises were conducted from 1986-1989 aboard U.S. National Oceanographic and Atmospheric Administration (NOAA) Research Vessels (R/V) Oceanographer and Discoverer and the Russia Far East Hydrometeorological Institute R/V Akademik Korolev. Table 1 presents the summary of the cruises.

Table 1. Summary of PMEL Cruises 1986 to 1989. The distance given is the distance over which data were collected along the cruise track.

YearCruise SectionResearch VesselPortsDatesDistance
(km)
Number
of
samples
1986EPOCSOceanographerBalboa - Honolulu
21 May-20 June
12,172
637
1986RITS/CO2OceanographerHonolulu-Kodiak
1 July-23 July
7,709
461
1987SAGA II, TransitAkademik KorolevHilo-Kuril Trench
1 May-8 May
4,503
218
1987SAGA II, Leg 1Akademik KorolevKuril Trench-Wellington
8 May-9 June
11,441
633
1987SAGA II, Leg 2Akademik KorolevWellington-Singapore12 June-6 July
11,912
501
1987TEW-3OceanographerTownsville-Kwajalein13 July-27 July
3,491
297
1987RITS/CO2OceanographerKwajalein-Seattle
29 July-28 August
10,520
669
1988RITS/CO2OceanographerDutch Harbor-Am. Samoa
6 April-5 May
8,648
668
1988EPOCSOceanographerAm. Samoa-Honolulu
9 May-4 June
8,492
547
1989RITS/CO2, Leg 1 DiscovererSeattle-Easter Island
5 February-1 March
7,097
398
1989RITS/CO2, Leg 2DiscovererEaster Island-Papeete
4 March-2 April
11,365
686
1989RITS/CO2, Leg 3DiscovererPapeete-Seattle
7 April-20 April
7,773
298
Total
105,123
6,013

The purpose of this report is to present the CO2 results and to show the calculations which have been used to convert the raw values to fugacities in units of microatmospheres (µatm).


akozyr 05/31/97