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Data accompanying the manuscript "Constraining the margin organic C flux" 

Organic carbon (OC) sedimentation in marine sediments is the largest long‐term sink of atmospheric CO2 after silicate weathering. Understanding the mechanistic and quantitative aspects of OC delivery and preservation in marine sediments is critical for predicting the role of the oceans in modulating global climate. Yet, estimates of the global OC sedimentation in marginal settings span an order of magnitude, and the primary controls of OC preservation remain highly debated. Here, we provide the first global bottom‐up estimate of OC sedimentation along the margins using a synthesis of literature data. We quantify both terrestrial‐ and marine‐sourced OC fluxes and perform a statistical analysis to discern the key factors influencing their magnitude. We find that the margins host 23.2 ± 3.5 Tmol of OC sedimentation annually, with approximately 84% of marine origin. Accordingly, we calculate that only 2%–3% of OC exported from the euphotic zone escapes remineralization before sedimentation. Surprisingly, over half of all global OC sedimentation occurs below bottom waters with oxygen concentrations greater than 180 μM, while less than 4% occurs in settings with <50 μM oxygen. This challenges the prevailing paradigm that bottom‐water oxygen (BWO) is the primary control on OC preservation. Instead, our statistical analysis reveals that water depth is the most significant predictor of OC sedimentation, surpassing all other factors investigated, including BWO levels and sea‐surface chlorophyll concentrations. This finding suggests that the primary control on OC sedimentation is not production, but the ability of OC to resist remineralization during transit through the water column and while settling on the seafloor. 

Cadmium (Cd) has a nutrient-like distribution in the ocean, similar to the macronutrient phosphate. Significant isotope fractionation induced by the biological cycling of Cd makes it a potential tracer for nutrients and productivity. However, the Cd flux and Cd isotope composition of marine sediments may also be influenced by local redox conditions and partial remineralization of organically hosted Cd. These confounding factors are under-constrained and render it challenging to use Cd as a reliable paleoproxy. To understand the relative importance of each of these processes, we examined the Cd isotope systematics of 69 modern sediments deposited across a wide range of environments. We complement these data with four profiles of particulate Cd isotope compositions from the Southern Ocean. We report three main results. First, we show that the sedimentary flux of Cd is tightly coupled to that of organic matter. Second, most Cd burial occurs in regions with some bottom-water oxygen, and the flux of CdS to anoxic regions is, globally, minor. Finally, we find that remineralization can substantially modify sedimentary Cd isotope compositions, though it is challenging to relate pelagic and sedimentary processes. For example, we find that the relationship between sedimentary Cd isotope compositions and surface seawater [Cd] is the reverse of that predicted by isotope reactor models. Likewise, sedimentary Cd isotope compositions are anti-correlated with bottom-water oxygen. While this pattern is consistent with preferential remineralization of isotopically heavy Cd, profiles of marine particulate matter reveal the reverse, whereby the Cd isotope composition of large particles, which are most likely to reach the seafloor, becomes increasingly ‘heavy’ with depth. These results highlight how productivity, redox, and remineralization all influence the flux and isotope composition of Cd to marine sediments. While our study suggests that there is no simple way to relate sedimentary Cd isotopes to surface nutrient utilization, our data point toward several potential controls that could form the basis of novel proxies for local redox conditions and remineralization. 

This is accompanying data for the manuscript "Refining the roles of productivity, redox, and remineralization on the cadmium isotope composition of marine sediments" 

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.