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Abstract An important role in the cycling of marine trace elements is scavenging, their adsorption and removal from the water column by sinking particles. Boundary scavenging occurs when areas of strong particle flux drive preferential removal of the trace metals at locations of enhanced scavenging. Due to its uniform production and quick burial via scavenging,²³⁰Th is used to assess sedimentary mass fluxes; however, these calculations are potentially biased near regions where net lateral transport of dissolved²³⁰Th violates the assumption that the flux of particulate²³⁰Th to the seabed equals its rate of production in the water column. Here, we present a water column transect of dissolved²³⁰Th along 152° W between Alaska and Tahiti (GEOTRACES GP15), where we examine²³⁰Th profiles across multiple biogeochemical provinces and, novelly, the lateral transport of²³⁰Th to distal East Pacific Rise hydrothermal plumes. We observed a strong relationship between the slope of dissolved²³⁰Th concentration‐depth profiles and suspended particle matter inventory in the upper‐mid water column, reinforcing the view that biogenic particle mass flux sets the background²³⁰Th distribution in open ocean settings. We find that, instead of the region of enhanced particle flux around the equator, hydrothermal plumes act as a regional boundary sink of²³⁰Th. At 152° W, we found that the flux‐to‐production ratio, and thereby error in²³⁰Th‐normalized sediment flux, is between 0.80 and 1.50 for hydrothermal water, but the error is likely larger approaching the East Pacific Rise. 

Abstract Hydrogen sulfide is produced by heterotrophic bacteria in anoxic waters and via carbonyl sulfide hydrolysis and phytoplankton emissions under oxic conditions. Apparent losses of dissolved cadmium (dCd) and zinc (dZn) in oxygen minimum zones (OMZs) of the Atlantic and Pacific Oceans have been attributed to metal‐sulfide precipitation formed via dissimilatory sulfate reduction. It has also been argued that such a removal process could be a globally important sink for dCd and dZn. However, our studies from the North Pacific OMZ show that dissolved and particulate sulfide concentrations are insufficient to support the removal of dCd via precipitation. In contrast, apparent dCd and dZn deficits in the eastern tropical South Pacific OMZ do reside in the oxycline with particulate sulfide maxima, but they also coincide with the secondary fluorescence maxima, suggesting that removal via sulfide precipitation may be due to a combination of dissimilatory and assimilatory sulfate reduction. Notably, dCd loss via precipitation with sulfide from assimilatory reduction was found in upper oxic waters of the North Pacific. While dissimilatory sulfate reduction may explain local dCd and dZn losses in some OMZs, our evaluation of North Pacific OMZs demonstrates that dCd and dZn losses are unlikely to be a globally relevant sink. Nevertheless, metal sulfide losses due to assimilatory sulfate reduction in surface waters should be considered in future biogeochemical models of oceanic Cd (and perhaps Zn) cycling. 

Abstract The physical and biogeochemical properties of the western Arctic Ocean are rapidly changing, resulting in cascading shifts to the local ecosystems. The nutrient‐rich Pacific water inflow to the Arctic through the Bering Strait is modified on the Chukchi and East Siberian shelves by brine rejection during sea ice formation, resulting in a strong halocline (called the Upper Halocline Layer (UHL)) that separates the cold and relatively fresh surface layer from the warmer and more saline (and nutrient‐poor) Atlantic‐derived water below. Biogeochemical signals entrained into the UHL result from Pacific Waters modified by sediment and river influence on the shelf. In this synthesis, we bring together data from the 2015 Arctic U.S. GEOTRACES program to implement a multi‐tracer (dissolved and particulate trace elements, radioactive and stable isotopes, macronutrients, and dissolved gas/atmospheric tracers) approach to assess the relative influence of shelf sediments, rivers, and Pacific seawater contribution to the Amerasian Arctic halocline. For each element, we characterized their behavior as mixing dominated (e.g., dCu, dGa), shelf‐influenced (e.g., dFe, dZn), or a combination of both (e.g., dBa, dNi). Leveraging this framework, we assessed sources and sinks contributing to elemental distributions: shelf sediments (e.g., dFe, dZn, dCd, dHg), riverine sources, (e.g., dCu, dBa, dissolved organic carbon), and scavenging by particles originating on the shelf (e.g., dFe, dMn, dV, etc.). Additionally, synthesized results from isotopic and atmospheric tracers yielded tracer age estimates for the Upper Halocline ranging between 1 and 2 decades on a spatial gradient consistent with cyclonic circulation.