An official website of the United States government
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.
more »
« less
Constraining the Global Ocean Cu Cycle With a Data‐Assimilated Diagnostic Model
Abstract Copper (Cu) is a biologically important trace metal for marine plankton, but it is also toxic at high concentrations. Understanding the global distribution of Cu and the processes controlling its cycling in the ocean is important for understanding how the distribution of this important element can respond to climate change. Here, we use available observations of dissolved copper, an artificial neural network, and an ocean circulation inverse model, to derive a global estimate of the three‐dimensional distribution and cycling of dissolved Cu in the ocean. We find that there is net removal by bio‐assimilation and/or scavenging of dissolved Cu in the surface ocean at a rate of ~1.7 Gmol yr−1and that both the concentration and export of dissolved Cu are highest in the Southern Ocean. In the subsurface above the near‐sediment layer, dissolved Cu is removed at a net rate of ~2.4 Gmol yr−1, consistent with scavenging onto sinking particles, contributing to an increase in the flux of particulate Cu with depth. This removal of Cu by scavenging in the interior ocean is balanced by a net near‐sediment source of dissolved Cu, which sustains a gradual increase in the concentration of dissolved Cu with depth. Globally, this net near‐sediment source is estimated at ~2.6 Gmol yr−1in the deep ocean and ~0.8 Gmol yr−1along continental shelves and slopes. Our results suggest an active oceanic dissolved Cu cycle with a mean internal ocean residence time of ~530 years, highlighting the potential for climate‐driven changes in the marine Cu cycle.
more »
« less
- Award ID(s):
- 1658392
- PAR ID:
- 10452822
- Publisher / Repository:
- DOI PREFIX: 10.1029
- Date Published:
- Journal Name:
- Global Biogeochemical Cycles
- Volume:
- 34
- Issue:
- 11
- ISSN:
- 0886-6236
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
-
Abstract The North Pacific has played an important role in ongoing discussions on the origin of the global correlation between oceanic dissolved Zn and Si, while data in the North Pacific have remained sparse. Here, we present dissolved Zn and δ66Zn data from the US GEOTRACES GP15 meridional transect along 152°W from Alaska to the South Pacific. In the south (<20°N) Zn and Si exhibit a tight linear correlation reflecting strong Southern Ocean influence, while in the north (>20°N) an excess of Zn relative to Si in upper and intermediate waters is due to regeneration of Zn together with PO4. Using a mechanistic model, we show that reversible scavenging is required as an additional process transferring Zn from the upper to the deep ocean, explaining the deep Zn maximum below the PO4maximum. This mechanism applied for reversible scavenging also provides an explanation for the observed isotope distribution: (a) fractionation during ligand binding and subsequent removal of residual heavy Zn in the upper ocean, drives the upper ocean toward lower δ66Zn, while (b) release of heavy Zn then coincides with the PO4maximum where carrier particles regenerate, causing a mid‐depth δ66Zn maximum. In the upper ocean, seasonal physical stratification is an additional important process influencing shallow δ66Zn signals. At the global scale, this mechanism invoking fractionation during ligand binding coupled with reversible scavenging offers a global explanation for isotopically light Zn at shallow depths and corresponding elevated mid‐depth δ66Zn signals, seen dominantly in ocean regions away from strong Southern Ocean control.more » « less
-
Abstract Aluminum (Al) is delivered to surface ocean waters by aeolian dust, making it a promising tracer to constrain dust deposition rates and the atmospheric supply of trace metal micronutrients. Over recent years, dissolved Al has been mapped along the GEOTRACES transects, providing unparalleled coverage of the world ocean. However, inferring atmospheric input rates from these observations is complicated by a suite of additional processes that influence the Al distribution, including reversible particle scavenging, biological uptake by diatoms, hydrothermal sources, sediment resuspension. Here we employ a data‐assimilation model of the oceanic Al cycle that explicitly accounts for these processes, allowing the atmospheric signal to be extracted. We conduct an ensemble of model optimizations that test different dust deposition distributions and consider spatial variations in Al solubility, thereby inferring the atmospheric Al supply that is most consistent with GEOTRACES observations. We find that 37.2 ± 11.0 Gmol/yr of soluble Al is added to the global ocean, dominated in the Atlantic Ocean, and that Al fractional solubility varies strongly as a function of atmospheric dust concentration. Our model also suggests that 6.1 ± 2.4 Gmol Al/yr is injected from hydrothermal vents, and that vertical Al redistribution through the water column is dominated by abiotic reversible scavenging rather than uptake by diatoms. Our results have important implications for the oceanic iron (Fe) budget: based on the soluble Fe:Al ratio of dust, we infer that aeolian Fe inputs lie between 3.82 and 9.25 Gmol/yr globally, and fall short of the biological Fe demand in most ocean regions.more » « less
-
The ratio of atmosphere-derived10Be to continent-derived9Be in marine sediments has been used to probe the long-term relationship between continental denudation and climate. However, its application is complicated by uncertainty in9Be transfer through the land-ocean interface. The riverine dissolved load alone is insufficient to close the marine9Be budget, largely due to substantial removal of riverine9Be to continental margin sediments. We focus on the ultimate fate of this latter Be. We present sediment pore-water Be profiles from diverse continental margin environments to quantify the diagenetic Be release to the ocean. Our results suggest that pore-water Be cycling is mainly controlled by particulate supply and Mn-Fe cycling, leading to higher benthic fluxes on shelves. Benthic fluxes may help close the9Be budget and are at least comparable to, or higher (~2-fold) than, the riverine dissolved input. These observations demand a revised model framework, which considers the potentially dominant benthic source, to robustly interpret marine Be isotopic records.more » « less
-
Abstract Sinking particles strongly regulate the distribution of reactive chemical substances in the ocean, including particulate organic carbon and other elements (e.g., P, Cd, Mn, Cu, Co, Fe, Al, and232Th). Yet, the sinking fluxes of trace elements have not been well described in the global ocean. The U.S. GEOTRACES campaign in the North Atlantic (GA03) offers the first data set in which the sinking flux of carbon and trace elements can be derived using four different radionuclide pairs (238U:234Th;210Pb:210Po;228Ra:228Th; and234U:230Th) at stations co‐located with sediment trap fluxes for comparison. Particulate organic carbon, particulate P, and particulate Cd fluxes all decrease sharply with depth below the euphotic zone. Particulate Mn, Cu, and Co flux profiles display mixed behavior, some cases reflecting biotic remineralization, and other cases showing increased flux with depth. The latter may be related to either lateral input of lithogenic material or increased scavenging onto particles. Lastly, particulate Fe fluxes resemble fluxes of Al and232Th, which all have increasing flux with depth, indicating a dominance of lithogenic flux at depth by resuspended sediment transported laterally to the study site. In comparing flux estimates derived using different isotope pairs, differences result from different timescales of integration and particle size fractionation effects. The range in flux estimates produced by different methods provides a robust constraint on the true removal fluxes, taking into consideration the independent uncertainties associated with each method. These estimates will be valuable targets for biogeochemical modeling and may also offer insight into particle sinking processes.more » « less
