Goodkin, Nathalie
(Ed.)
Abstract Most oceanic lead (Pb) is from anthropogenic emissions into the atmosphere deposited into surface waters, mostly during the past two centuries. The space‐ and time‐dependent emission patterns of anthropogenic Pb (and its isotope ratios) constitute a global geochemical experiment providing information on advective, mixing, chemical, and particle flux processes redistributing Pb within the ocean. Pb shares aspects of its behavior with other elements, for example, atmospheric input, dust solubilization, biological uptake, and reversible exchange between dissolved and adsorbed Pb on sinking particles. The evolving distributions allow us to see signals hidden in steady‐state tracer distributions. The global anthropogenic Pb emission experiment serves as a tool to understand oceanic trace element dynamics. We obtained a high‐resolution (5° station spacing) depth transect of dissolved Pb concentrations and Pb isotopes from Alaska (55°N) to just north of Tahiti (20°S) near 152°W longitude. The sections reveal distinct sources of Pb (American, Australian, and Chinese), transport of Australian style Pb to the water mass formation region of Sub‐Antarctic Mode Water which is advected northward, columnar Pb isotope contours due to reversible particle exchange on sinking particles from high‐productivity particle veils, and a gradient of high northern deep water [Pb] to low southern deep water [Pb] that is created by reversible exchange release of Pb from sinking particles carrying predominantly northern hemisphere Pb.208Pb/206Pb versus206Pb/207Pb isotope relationships show that most oceanic Pb in the North Pacific is from Chinese and American sources, whereas Pb in the South Pacific is from Australian and American sources.
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