J. Radfordknoery et Ga. Cutter, BIOGEOCHEMISTRY OF DISSOLVED HYDROGEN-SULFIDE SPECIES AND CARBONYL SULFIDE IN THE WESTERN NORTH-ATLANTIC OCEAN, Geochimica et cosmochimica acta, 58(24), 1994, pp. 5421-5431
The biogeochemistry of total sulfide dissolved in the open ocean is a
poorly understood component of the global sulfur cycle. Here, the cycl
ing of total sulfide was examined in the western North Atlantic Ocean
using specially developed sampling and analytical methods. Total sulfi
de (particulate + dissolved sulfide) concentrations ranged from <2-550
pmol/L; concentrations were highest in the mixed layer and decreased
with depth. Significant levels (up to 19 pmol/L) of free sulfide (unco
mplexed sulfide) were determined in the top 50 m of the water column.
Sources of total sulfide were examined. in particular, the rate of car
bonyl sulfide (OCS) hydrolysis was redetermined under oceanographic co
nditions, and the depth distribution of OCS was examined. The patterns
of near-surface enrichment (up to 150 pmol/L) and depletion at depth
observed in OCS depth profiles suggest in situ production of OCS. To q
uantify the sources and sinks of total sulfide in the mixed layer of t
he Sargasso Sea, a budget was constructed. The rate of total sulfide p
roduction was 5.5 pmol L(-1) h(-1) (OCS hydrolysis + atmospheric input
), and total sulfide removal rate was 115 pmol L(-1) h(-1) (oxidation
+ particulate sinking). The significant difference between the known s
ources and sinks indicates that other processes are important for the
cycling of sulfide. Similarities in the depth distribution of total su
lfide and chlorophyll a, and results from recent laboratory experiment
s argue strongly in favor of biological involvement in the production
of total sulfide in the open ocean.