Description: Previous work showed that South Atlantic sediments have lower glacial than Holocene 231Pa/230Th, which was attributed to a switch in the flow direction of Atlantic deep-water. Debate exists, however as to the degree to which two processes - circulation and scavenging - determine sedimentary 231Pa/230Th, making this interpretation contentious. Here we address this issue using 145-kyr records of paleocirculation proxies. Benthic foraminiferal d13C, neodymium isotopes (ENd) and sedimentary 231Pa/230Th were all measured in a single sediment core from the South Atlantic subtropical gyre. This site largely excludes the influence of local productivity changes on 231Pa/230Th records. Measured 231Pa/230Th ranges between ~0.041 during glacials to ~0.055 during interglacial periods and are consistently lower than the production ratio, indicating export of 231Pa from the central South Atlantic for the entire duration of the record. The lower glacial 231Pa/230Th is regionally consistent, suggesting that basin-scale oceanographic processes cause the decrease. In turn, less radiogenic ENd and lower benthic d13C confirm the classical picture of an increase in Southern Component Water (SCW) influence in the Atlantic during glacial periods and point to a circulation control on the observed 231Pa/230Th decrease rather than a local productivity change. We suggest that associated with this change in water mass distribution the dominant sink for 231Pa shifted from the margins of the South Atlantic and/or the Southern Ocean during interglacials, to the North Atlantic during glacial periods. Indeed, elevated 231Pa/230Th in the deep North Atlantic during glacials supports this mechanism of northward transport of 231Pa by SCW.

Description: The GEOTRACES Intermediate Data Product 2017 (IDP2017) is the second publicly available data product of the international GEOTRACES programme, and contains data measured and quality controlled before the end of 2016. The IDP2017 includes data from the Atlantic, Pacific, Arctic, Southern and Indian oceans, with about twice the data volume of the previous IDP2014. For the first time, the IDP2017 contains data for a large suite of biogeochemical parameters as well as aerosol and rain data characterising atmospheric trace element and isotope (TEI) sources. The TEI data in the IDP2017 are quality controlled by careful assessment of intercalibration results and multi-laboratory data comparisons at crossover stations. The IDP2017 consists of two parts: (1) a compilation of digital data for more than 450 TEIs as well as standard hydrographic parameters, and (2) the eGEOTRACES Electronic Atlas providing an on-line atlas that includes more than 590 section plots and 130 animated 3D scenes. The digital data are provided in several formats, including ASCII, Excel spreadsheet, netCDF, and Ocean Data View collection. Users can download the full data packages or make their own custom selections with a new on-line data extraction service. In addition to the actual data values, the IDP2017 also contains data quality flags and 1-σ data error values where available. Quality flags and error values are useful for data filtering and for statistical analysis. Metadata about data originators, analytical methods and original publications related to the data are linked in an easily accessible way. The eGEOTRACES Electronic Atlas is the visual representation of the IDP2017 as section plots and rotating 3D scenes. The basin-wide 3D scenes combine data from many cruises and provide quick overviews of large-scale tracer distributions. These 3D scenes provide geographical and bathymetric context that is crucial for the interpretation and assessment of tracer plumes near ocean margins or along ridges. The IDP2017 is the result of a truly international effort involving 326 researchers from 22 countries. This publication provides the critical reference for unpublished data, as well as for studies that make use of a large cross-section of data from the IDP2017.

Description: The GEOVIDE cruise, a collaborative project within the framework of the international GEOTRACES programme, was conducted along the French-led section in the North Atlantic Ocean (Section GA01), between 15 May and 30 June 2014. In this Special Issue, results from GEOVIDE, including physical oceanography and trace element and isotope cyclings, are presented among seventeen articles. Here, the scientific context, project objectives and scientific strategy of GEOVIDE are provided, along with an overview of the main results from the articles published in the special issue.

Description: Human activity is altering the ocean. This is happening through climate change, the release of pollutants, and direct exploitation of the marine environment. Recent advances in understanding the chemical cycling of trace elements within the global ocean comes at a critical time. Society is now increasingly viewing the ocean as a resource while also recognising that ocean systems are vulnerable to change.

Description: Quantifying fluxes of trace elements and their isotopes (TEIs) at the ocean's sediment–water boundary is a pre-eminent challenge to understand their role in the present, past and future ocean. There are multiple processes that drive the uptake and release of TEIs, and properties that determine their rates are unevenly distributed (e.g. sediment composition, redox conditions and (bio)physical dynamics). These factors complicate our efforts to find, measure and extrapolate TEI fluxes across ocean basins. GEOTRACES observations are unveiling the oceanic distributions of many TEIs for the first time. These data evidence the influence of the sediment–water boundary on many TEI cycles, and underline the fact that our knowledge of the source–sink fluxes that sustain oceanic distributions is largely missing. Present flux measurements provide low spatial coverage and only part of the empirical basis needed to predict TEI flux variations. Many of the advances and present challenges facing TEI flux measurements are linked to process studies that collect sediment cores, pore waters, sinking material or seawater in close contact with sediments. However, such sampling has not routinely been viable on GEOTRACES expeditions. In this article, we recommend approaches to address these issues: firstly, with an interrogation of emergent data using isotopic mass-balance and inverse modelling techniques; and secondly, by innovating pursuits of direct TEI flux measurements. We exemplify the value of GEOTRACES data with a new inverse model estimate of benthic Al flux in the North Atlantic Ocean. Furthermore, we review viable flux measurement techniques tailored to the sediment–water boundary. We propose that such activities are aimed at regions that intersect the GEOTRACES Science Plan on the basis of seven criteria that may influence TEI fluxes: sediment provenance, composition, organic carbon supply, redox conditions, sedimentation rate, bathymetry and the benthic nepheloid inventory.

Description: Highlights • Novel approach to constrain past export production using Ba isotopes. • Ba isotopes improve reliability of the Ba accumulation productivity proxy. • Higher productivity during PETM recovery contributed to rapid carbon sequestration. Abstract The Paleocene–Eocene thermal maximum (PETM; ∼56 Ma) was a transient global warming event associated with a huge perturbation to the global carbon cycle. Changes in marine biological productivity may have contributed to the rapid recovery from this climate change event, by driving the burial of inorganic and organic carbon. Disagreement between proxy reconstructions, however, makes the response of biological productivity to climatic changes experienced during the PETM uncertain. Accumulation of non-detrital barium (Ba) in marine sediments is a commonly used proxy for export production. This proxy however can be compromised by artifacts resulting from dilution and changes in barite preservation, issues that have been debated for its application to sediments deposited during the PETM. Here we present a new approach to address these limitations, by combining non-detrital Ba accumulation with Ba isotope data for marine PETM sediments. Observed positive correlation between these variables is consistent with their control by local changes in export production. These results help resolve previous discrepancies between productivity reconstructions, and indicate export production at sites in the Southern Ocean and South Atlantic decreased or remained unchanged following the PETM onset, followed by an increase to maximum values in the PETM recovery period. This increase in export production coincides with elevated carbonate accumulation rates, representing an important mode of carbon sequestration. These new constraints therefore support the idea that increased production and export of calcifying nannoplankton, perhaps driven by changes in ocean stratification and/or terrestrial runoff, played an important role in rapid recovery from the PETM. This work also demonstrates the utility of sedimentary Ba isotope compositions for understanding past changes in the marine carbon cycle.

Description: Barium has been used as a biogeochemical tracer for alkalinity, productivity, and riverine inputs in the ocean, but its oceanic cycle remains poorly constrained. Barium stable isotope measurements may improve the use of Ba as a tracer and better constrain the cycling of Ba, but data are only available in limited regions of the oceans. In this study, we present dissolved seawater Ba isotopic compositions in a sample collection spanning the North Atlantic, South Atlantic, North Pacific and Southern Oceans. Compiled global upper-ocean [Ba] data show a relatively constant [Ba] (35–45nM) in the near-surface waters throughout the global ocean, with the exception of areas near river inputs or strong upwelling. The relatively uniform distribution of [Ba] in the upper ocean seawater indicates that Ba removal is slow relative to supply and mixing, and implies that near-surface Ba isotope values are controlled by basin-scale balances rather than by regional or short-term processes. Seawater Ba isotopic compositions show a large variation of δ138/134Bavalues ranging from 0.24 to 0.65�, and a tight relationship with [Ba]. This global relationship can be simply modelledassuming a primary deep Southern Ocean source for Ba to yield a maximum isotope fractionation of α=1.00058 ±0.00010(α=138/134Baseawater/138/134Baparticle). This suggested isotope fractionation during Ba removal from seawater is larger than implied by laboratory measurement during barite formation, suggesting additional fractionating phases or a two-stage fractionation process. Riverine input from the Rio de la Plata to the South Atlantic has a signature of δ138/134Ba=−0.06–0.11‰, which is too light to explain the heavy values (〉0.58‰) observed in the surface open ocean. Globally, the Ba isotope composition of the upper ocean waters is correlated with the fraction of Ba utilization at the basin scale (which varies from 〈15 to 70% at sites studied here). In the deep Atlantic Ocean, distinct δ138/134Basignals in the northern-sourced (≈0.45‰) and the southern-sourced water (≈0.25‰) trace mixing and allow identification of non-conservative behaviourof Ba, reflecting additional inputs or sinks of Ba during transport (most likely addition from sediment or hydrothermal). Ba isotopes may be useful to trace such inputs in the present and past ocean.