Description: Beryllium isotopes have emerged as a quantitative tracer of continental weathering, but accurate and precise determination of the cosmogenic 10 Be and stable 9 Be in seawater is challenging, because seawater contains high concentrations of matrix elements but extremely low concentrations of 9 Be and 10 Be. In this study, we develop a new, time‐efficient procedure for the simultaneous preconcentration of 9 Be and 10 Be from (coastal) seawater based on the iron co‐precipitation method. The concentrations of 9 Be, 10 Be, and the resulting 10 Be/ 9 Be ratio for Changjiang Estuary water derived from the new procedure agree well with those obtained from the conventional procedure requiring separate preconcentration for 9 Be and 10 Be determinations. By avoiding the separate preconcentration, our newly developed procedure contributes toward more time‐efficient handling of samples, less sample cross‐contamination, and a more reliable 10 Be/ 9 Be ratio. Prior to this, we validated the iron co‐precipitation method using artificial seawater and natural water samples from the Amazon Estuary regarding: (1) the “matrix effect” for Be analysis, (2) its extraction efficiency for pg g −1 levels Be in the presence and absence of organic matter, and (3) the data comparability with another preconcentration method. We calculated that for the determination of 9 Be and 10 Be in most open ocean seawater with typical 10 Be concentrations of 〉 500 atoms g −1 , good precisions (〈 5%) can be achieved using less than 3 liters of seawater compared to more than 20 liters routinely used previously. Even for coastal seawater with extremely low 10 Be concentration (e.g., 100 atoms g −1 ), we estimate a maximum amount of 10 liters to be adequate.

Description: Highlights • Negligible Ba removal observed in the Rainbow hydrothermal system. • Insignificant modification of Ba isotope composition of the vent fluid endmember. • Rainbow vent introduces isotopically light Ba (−0.17) to the deep Atlantic Ocean. • Hydrothermal inputs contribute 4.6 ± 2.2 Gmol/yr Ba to the ocean. Abstract The marine barium (Ba) cycle is closely connected to the short-timescale carbon cycle, and Ba serves as a valuable paleo proxy for export production, ocean alkalinity, and terrestrial inputs. However, the marine Ba budget is poorly constrained, particularly regarding the fluxes of hydrothermally sourced Ba, which hinders our understanding of the Ba cycle and use of Ba-based proxies. Recent studies have suggested a modern source-sink imbalance of Ba isotopes in the global ocean, with sources being overall isotopically heavier than the sinks, and the hydrothermal Ba inputs were considered isotopically heavy sources. In this study, we present the first investigation of Ba and its isotopes in a non-buoyant hydrothermal plume based on dissolved and particulate samples collected from the Rainbow hydrothermal vent field on the Mid-Atlantic Ridge. Our data reveal strong hydrothermal signals at near-field stations, as evidenced by helium isotopes, accompanied by elevated concentrations of dissolved and particulate Ba. Dissolved Ba isotope compositions (δ138Ba) in hydrothermally influenced deep waters (∼0.3 ) are lighter than at similar depths of far-field stations (∼0.45 ) in the Atlantic Ocean. The concentrations and isotopic compositions of dissolved and labile particulate Ba in the non-buoyant hydrothermal plume can be explained by conservative mixing between a Ba-enriched hydrothermal component and North Atlantic Deep Water. By extrapolating the correlations to the vent fluid endmember, our results suggest that there is negligible removal of Ba, and insignificant modification of Ba isotopic signatures, from the vent fluid endmember to the non-buoyant hydrothermal plume. This indicates that the Rainbow hydrothermal system introduces isotopically light Ba (−0.17 ± 0.05 ) to the deep Atlantic Ocean. We estimate that global hydrothermal inputs of Ba are 4.6 ± 2.2 Gmol/yr. These observations highlight the potential of hydrothermal Ba to be an isotopically light source component of the marine Ba isotope budget.

Description: Black shale sediments from the Barremian to Aptian South Atlantic document intense and widespread burial of marine organic carbon during the initial stages of seafloor spreading between Africa and South America. The enhanced sequestration of atmospheric CO2 makes these young ocean basins potential drivers of the Early Cretaceous carbon cycle and climate perturbations. The opening of marine gateways between initially restricted basins and related circulation and ventilation changes are a commonly invoked explanation for the transient formation and disappearance of these regional carbon sinks. However, large uncertainties in paleogeographic reconstructions limit the interpretation of available paleoceanographic data and prevent any robust model-based quantifications of the proposed circulation and carbon burial changes. Here, we present a new approach to assess the principal controls on the Early Cretaceous South Atlantic and Southern Ocean circulation changes under full consideration of the uncertainties in available boundary conditions. Specifically, we use a large ensemble of 36 climate model experiments to simulate the Barremian to Albian progressive opening of the Falkland Plateau and Georgia Basin gateways with different configurations of the proto-Drake Passage, the Walvis Ridge, and atmospheric CO2 concentrations. The experiments are designed to complement available geochemical data across the regions and to test circulation scenarios derived from them. All simulations show increased evaporation and intermediate water formation at subtropical latitudes that drive a meridional overturning circulation whose vertical extent is determined by the sill depth of the Falkland Plateau. Densest water masses formed in the southern Angola Basin and potentially reached the deep Cape Basin as Walvis Ridge Overflow Water. Paleogeographic uncertainties are as important as the lack of precise knowledge of atmospheric CO2 levels for the simulated temperature and salinity spread in large parts of the South Atlantic. Overall temperature uncertainties are up to 15 °C and increase significantly with water depth. The ensemble approach reveals temporal changes in the relative importance of geographic and radiative forcings for the simulated oceanographic conditions and, importantly, nonlinear interactions between them. Progressive northward opening of the highly restricted Angola Basin increased the sensitivity of local overturning and upper ocean stratification to atmospheric CO2 concentrations due to large-scale changes in the hydrological cycle, while the chosen proto-Drake Passage depth is critical for the ocean dynamics and CO2 response in the southern South Atlantic. Finally, the simulated processes are integrated into a recent carbon burial framework to document the principal control of the regional gateway evolution on the progressive shift from the prevailing saline and oxygen-depleted subtropical water masses to the dominance of ventilated high-latitude deep waters.

Description: The datasets contains benthic foraminiferal oxygen isotope (δ¹⁸O) records of sediment core NGHP 17, retrieved in the Bay of Bengal. The record covers the last ~1 million years. C. wuellerstorfi and C. mundulus are epibenthic foraminiferal species, and δ¹⁸O values were adjusted to equilibrium by adding 0.64 following Shackleton et al. (1984).