Lg. Anderson et al., Annual carbon fluxes in the upper Greenland Sea based on measurements and a box-model approach, TELLUS B, 52(3), 2000, pp. 1013-1024
Measurements of nitrate and the carbonate system parameters performed mainl
y From 1993 to 1997 have been used to estimate the evolution of the concent
ration fields over the year in the surface and underlying waters of the cen
tral Greenland Sea. This, together with synoptic surface wind data From the
NCEP/NCAR reanalysis project, is used to evaluate the vertical mixing, the
biological production and decay, as well as the air-sea exchange of CO2 in
the region. Tn the winter season, the vertical mixing dominates the change
of the nitrate concentration in the surface water. The mixing factor estim
ated for this season is used to compute the addition of chemical constituen
ts to the surface water from below. The residual nitrate concentration chan
ge, after the mixing contribution has been subtracted, is attributed to bio
logical production or decay. The computations are performed with a 1-day re
solution and initially the advective contribution is neglected, as the hori
zontal gradients in the central Greenland Sea gyre are small. Following thi
s approach, the air sea flux of CO2 is directed into the sea all year aroun
d, with an annual uptake of 53 +/- 4 g C m(-2) yr(-1) for the years 93 to 9
7. The carbon flux as driven by biology shows a strong primary production p
eak around Julian day 140 followed by a decrease which turns into decay of
organic matter at about day 200. Summarizing the biological activity in the
surface water over the year gives a new production of 34 g C m(-2) yr(-1).
The vertical flux of dissolved inorganic carbon into the surface water fro
m below amounts to 11 g C m(-2) yr(-1). The build up of carbon in the surfa
ce water, 30 g C m(-2) yr(-1), is explained by that the temperature of the
outflowing water is approximately 2 degrees C colder than the inflowing wat
er, giving a higher dissolved inorganic carbon concentration as a result of
the increase in the solubility of carbon.