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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 dissolved 230Th/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 initial 230Th/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.

Abstract Black carbon is a refractory form of organic carbon formed from the incomplete combustion of fossil fuels and biomass. Riverine transport is considered the dominant pathway of black carbon to the coastal oceans. However, the provenance and pathways of black carbon to the open ocean remain unknown. Here we use both stable and radiogenic isotopes of carbon to show that sedimentary black carbon across the equatorial Atlantic Ocean is aeolian and primarily derived from biomass burning of C4-plants. Fluxes of surface sedimentary black carbon measured along an equatorial Atlantic Ocean transect using chemothermal oxidation at 375 °C were relatively consistent across the Atlantic, ranging from 0.10–0.35 mg cm−2 kyr−1. Carbon isotope values near Africa suggest the black carbon was mostly young and derived from C4 plants, whereas offshore South America, the black carbon was older and dominated by C3 plants. The black carbon radiocarbon values were similar to the reservoir corrected total organic carbon near Africa, implying little pre-aging on land and increased westwards. These findings highlight the influence of C4-biomass burning in the tropical Atlantic and the importance of aeolian deposition as a black carbon source within the global carbon cycle.

Abstract Past studies of noble gas concentrations in the deep ocean have revealed widespread, several percent undersaturation of Ar, Kr, and Xe. However, the physical explanation for these disequilibria remains unclear. To gain insight into undersaturation set by deep‐water formation, we measured heavy noble gas isotope and elemental ratios from the deep North Pacific using a new analytical technique. To our knowledge, these are the first high‐precision seawater profiles of 38Ar/36Ar and Kr and Xe isotope ratios. To interpret isotopic disequilibria, we carried out a suite of laboratory experiments to measure solubility fractionation factors in seawater. In the deep North Pacific, we find undersaturation of heavy‐to‐light Ar and Kr isotope ratios, suggesting an important role for rapid cooling‐driven, diffusive air‐to‐sea gas transport in setting the deep‐ocean undersaturation of heavy noble gases. These isotope ratios represent promising new constraints for quantifying physical air‐sea gas exchange processes, complementing noble gas concentration measurements.