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.
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Calculating Sedimentation Rates of Oxic Pelagic Clays Using Core Top Thorium Isotopes
Abstract Oxic pelagic clays are an important component of seafloor sediment that may hold valuable information about past ocean chemistry due to their affinity for and accumulation of biogeochemically important metals. We present a new approach to calculating site‐specific sedimentation rates (SRs) by comparing authigenic sediment thorium isotope compositions (230Th/232Th) to seawater dissolved230Th/232Th in a suite of deep (>3,000 m) pelagic core sites. We extracted the authigenic sediment fraction using an HHAc leach protocol, which major element chemistry (Al, Mn, Fe, Ti) suggested was less affected by lithogenic contamination than the HCl leach. Four different methods were tested for extracting the appropriate initial230Th/232Th from seawater: using either the nearest water column station (methods 1 and 2) or a regionally averaged profile (methods 3 and 4) and using either the bottommost profile measurement (methods 1 and 3) or linear regression of the profile and extrapolation to the seafloor (methods 2 and 4). Method 3 outperformed the other methods in reconstructing previously published SRs from pelagic clays in the North Pacific. The new thorium‐based SRs were then combined with estimates from the total sediment thickness on ocean crust and non‐lithogenic cobalt accumulation to determine the best estimates for SRs of oxic pelagic clays. The Pacific has the lowest SR (median 0.28 cm/kyr), while the Atlantic is higher (median 0.46 cm/kyr) and the Indian Ocean is highest (median 0.75 cm/kyr). These new estimates are consistent with the expected spatial patterns of sedimentation, but they revise the absolute SR values downward from available gridded SR maps.
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- Award ID(s):
- 1948716
- PAR ID:
- 10568051
- Publisher / Repository:
- DOI PREFIX: 10.1029
- Date Published:
- Journal Name:
- Geochemistry, Geophysics, Geosystems
- Volume:
- 26
- Issue:
- 1
- ISSN:
- 1525-2027
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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