Mercury concentration and speciation were measured in surface and deep ocea
n waters of the South and equatorial Atlantic. In the surface waters, total
Hg was 2.9 +/- 1.7 pM on average, with a significant fraction present as r
eactive Hg (1.7 +/- 1.2 pM). The reactive Hg fraction consisted of elementa
l Hg (Hg degrees) as the dominant species (1.2 +/- 0.8 pM). Measurements in
surface waters also showed that Hg partitioned to the "colloidal" phase (0
.33 +/- 0.28 pM) and was associated with particulate matter (0.1 +/- 0.05 p
M), No dimethylmercury (DMHg < 0.01 pM) or monomethylmercury (MMHg; < 0.05
pM) was detected in mixed layer samples. The highest DMHg concentrations we
re found in recently formed deep waters - Antarctic Intermediate Water and
Antarctic Bottom Water and in the equatorial subthermocline region, Higher
concentrations of DMHg coincided with higher values of apparent oxygen util
ization, indicative of a link between microbial activity and methylated Hg
production, The lowest-deep water DMHg concentrations were found in the cor
e of the North Atlantic Deep Water. Incubation experiments on-board demonst
rated that light enhanced the decomposition of DMHg, with MMHg as the major
product. In deep waters, Hg degrees was still an important constituent and
is likely formed as a decomposition product from MMHg. These results sugge
st that methylated Hg production occurs primarily in regions of high biolog
ical activity, and that ionic Hg is strongly complexed to organic matter (c
olloidal material) in open ocean surface waters. (C) 1999 Elsevier Science
Ltd. All rights reserved.