Description: Based on an unprecedented dissolved barium (D_Ba) data set collected in the Mediterranean Sea during a zonal transect between the Lebanon coast and Gibraltar (M84/3 cruise, April 2011), we decompose the D_Ba distribution to isolate the contribution of biogeochemical processes from the impact of the oceanic circulation. We have built a simple parametric water mass analysis (Parametric Optimum Multiparameter analysis) to reconstruct the contribution of the different Mediterranean water masses to the thermohaline structure. These water mass fractions have then been used to successfully reconstruct the background vertical gradient of D_Ba reflecting the balance between the large-scale oceanic circulation and the biological activity over long time scales. Superimposed on the background field, several D_Ba anomalies have been identified. Positive anomalies are associated with topographic obstacles and may be explained by the dissolution of particulate biogenic barium (P_Ba barite) of material resuspended by the local currents. The derived dissolution rates range from 0.06 to 0.21 μmol m−2 d−1. Negative anomalies are present in the mesopelagic region of the western and eastern basins (except in the easternmost Levantine basin) as well as in the abyssal western basin. This represents the first quantification of the nonconservative component of the D_Ba signal. These mesopelagic anomalies could reflect the subtraction of D_Ba during P_Ba barite formation occurring during organic carbon remineralization. The deep anomalies may potentially reflect the transport of material toward the deep sea during winter deep convection and the subsequent remineralization. The D_Ba subtraction fluxes range from −0.07 to −1.28 μmol m−2 d−1. D_Ba-derived fluxes of P_Ba barite (up to 0.21 μmol m−2 d−1) and organic carbon (13 to 29 mmol C m−2 d−1) are in good agreement with other independent measurements suggesting that D_Ba can help constrain remineralization horizons. This study highlights the importance of quantifying the impact of the large-scale oceanic circulation in order to better understand the biogeochemical cycling of elements and to build reliable geochemical proxies.

Description: Anthropogenic activities have resulted in enhanced lead (Pb) emissions to the environment over the past century, mainly through the combustion of leaded gasoline. Here, we present the first combined dissolved (DPb), labile (LpPb) and particulate (PPb) Pb dataset from the Northeast Atlantic (Celtic Sea) since the phasing out of leaded gasoline in Europe. Concentrations of DPb in surface waters have decreased by 4-fold over the last four decades. We demonstrate that anthropogenic Pb is transported from the Mediterranean Sea over long distances (〉2500 km). Benthic DPb fluxes exceeded the atmospheric Pb flux in the region, indicating the importance of sediments as a contemporary Pb source. A strong positive correlation between DPb, PPb and LpPb indicates a dynamic equilibrium between the phases and the potential for particles to ‘buffer’ the DPb pool. This study provides insights into Pb biogeochemical cycling and demonstrates the potential of Pb in constraining ocean circulation patterns.

Description: The South China Sea (SCS) is the largest semienclosed marginal sea in the western Pacific (WP) and connects to the west Pacific through the Luzon Strait (LU). In this study, we use the observation of transient tracer chlorofluorocarbon‐12 (CFC‐12) to calculate the ventilation time scales of the SCS, LU, and WP. The CFC‐12 and oxygen data are used together to identify the sandwiched structure vertically of the flows across the LU. The CFC‐12 and oxygen distributions reveal a pronounced decrease westward across the LU and a slight decrease southward in the transport of the SCS. The mean age gradient of the salinity minimum (Smin) water between the WP and the northern SCS could be a consequence of intensive mixing and entrainment of the inflow water from the WP. An expected difference in age between the LU and SSCS is verified to reflect the transit time for the given water layers in the SCS. Thus, a mean transit time of 77 ± 20 years is estimated for the intermediate water in the SCS interior.

Description: Transient tracer measurements can constrain the rates and pathways of ocean ventilation and act as proxies for biogeochemically relevant gases such as CO2 and oxygen. Various techniques have deduced changes in ocean ventilation over decadal timescales using transient tracer measurements made on repeat sections, but these require a priori assumptions about mixing in the ocean interior. Here, we introduce a simple, direct observational method that takes advantage of the similar atmospheric increase rates of chlorofluorocarbon-12 and sulfur hexafluoride, but with a time lag (offset) of 1415 years. Such repeat measurements can be directly compared without prior assumptions about mixing. A difference larger than similar to 2 years between modern sulfur hexafluoride and historical chlorofluorocarbon-12 tracer ages implies a change in ventilation, although lack of difference does not necessarily imply no change. Several tracer data sets are presented, which suggest changes in ventilation in the South Pacific and North Atlantic Oceans.

Description: The temporal dynamics of the concentrations of nitrate (N), phosphate (P), and the N:P ratio in the upper water column (200-600m) of the Mediterranean (MED) Sea were investigated using observational data (~123,100 data points) collected between 1985 and 2014. The studied variables were found to evolve similarly in the western and eastern MED Sea. In both basins, the N concentration increased during the first part of the observational period (1985-1998), and the temporal trend of N was broadly consistent with the history of riverine and atmospheric nitrogen input from populated areas in Europe, with a lag period of 20years. In subsequent years, the N concentration was high and relatively constant between 1998 and 2005, after which N decreased gradually, although the decreasing trend was indistinct in the western basin. In particular, the trend of constant then declining N after 1998 is consistent with the history of pollutant nitrogen emissions from the European continent, allowing a 20 year lag following the introduction of regulation of pollutant nitrogen in the 1970s. The three-phase temporal transition in P in both basins was more consistent with the riverine phosphorus input, with a lag period of 20years. Our analysis indicates that the recent dynamics of N and P in the upper MED Sea has been sensitive to the dynamics of anthropogenic nitrogen and phosphorus input from atmospheric deposition and rivers

Description: The variability of the Atlantic Meridional Overturning Circulation (AMOC) has considerable impacts on the global climate system. Past studies have shown that changes in the South Atlantic control the stability of the AMOC and drive an important part of its variability. That is why significant resources have been invested in a South (S)AMOC observing system. In January 2017, the RV Maria S. Merian conducted the first GO‐SHIP hydrographic transect along the SAMOC‐Basin Wide Array (SAMBA) line at 34.5°S in the South Atlantic. This paper presents estimates of meridional volume, freshwater (MFT), and heat (MHT) transports through the line using the slow varying geostrophic density field and direct velocity observations. An upper and an abyssal overturning cell are identified with a strength of 15.64 ± 1.39 Sv and 2.4 ± 1.6 Sv, respectively. The net northward MHT is 0.27 ± 0.10 PW, increasing by 0.12 PW when we remove the observed mesoscale eddies with a climatology derived from the Argo floats data set. We attribute this change to an anomalous predominance of cold core eddies during the cruise period. The highest velocities are observed in the western boundary, within the Brazil and the Deep Western Boundary currents. These currents appear as a continuous deep jet located 150 km off the slope squeezed between two cyclonic eddies. The zonal changes in water masses properties and velocity denote the imprint of exchange pathways with both the Southern and the Indian oceans. Key Points: ● Overturning maximum is 15.64 ± 1.39 Sv; Meridional heat and freshwater transport are 0.27 ± 0.10 PW and 0.23 ± 0.02 Sv, respectively ● Excluding the mesoscale eddies from the section increased the meridional heat transport by 0.12 PW ● The distribution of water masses and currents reflects the favorable position of the section for observing

Description: Fossil fuel combustion, land use change and other human activities have increased the atmospheric carbon dioxide (CO2) abundance by about 50% since the beginning of the industrial age. The atmospheric CO2 growth rates would have been much larger if natural sinks in the land biosphere and ocean had not removed over half of this anthropogenic CO2. As these CO2 emissions grew, uptake by the ocean increased in response to increases in atmospheric CO2 partial pressure (pCO(2)). On land, gross primary production also increased, but the dynamics of other key aspects of the land carbon cycle varied regionally. Over the past three decades, CO2 uptake by intact tropical humid forests declined, but these changes are offset by increased uptake across mid- and high-latitudes. While there have been substantial improvements in our ability to study the carbon cycle, measurement and modeling gaps still limit our understanding of the processes driving its evolution. Continued ship-based observations combined with expanded deployments of autonomous platforms are needed to quantify ocean-atmosphere fluxes and interior ocean carbon storage on policy-relevant spatial and temporal scales. There is also an urgent need for more comprehensive measurements of stocks, fluxes and atmospheric CO2 in humid tropical forests and across the Arctic and boreal regions, which are experiencing rapid change. Here, we review our understanding of the atmosphere, ocean, and land carbon cycles and their interactions, identify emerging measurement and modeling capabilities and gaps and the need for a sustainable, operational framework to ensure a scientific basis for carbon management.

Description: The oceanic uptake and resulting storage of the anthropogenic CO2 (Cant) that humans have emitted into the atmosphere moderates climate change. Yet our knowledge about how this uptake and storage has progressed in time remained limited. Here, we determine decadal trends in the storage of Cant by applying the eMLR(C*) regression method to ocean interior observations collected repeatedly since the 1990s. We find that the global ocean storage of Cant grew from 1994 to 2004 by 29 ± 3 Pg C dec−1 and from 2004 to 2014 by 27 ± 3 Pg C dec−1 (±1σ). The storage change in the second decade is about 15 ± 11% lower than one would expect from the first decade and assuming proportional increase with atmospheric CO2. We attribute this reduction in sensitivity to a decrease of the ocean buffer capacity and changes in ocean circulation. In the Atlantic Ocean, the maximum storage rate shifted from the Northern to the Southern Hemisphere, plausibly caused by a weaker formation rate of North Atlantic Deep Waters and an intensified ventilation of mode and intermediate waters in the Southern Hemisphere. Our estimates of the Cant accumulation differ from cumulative net air-sea flux estimates by several Pg C dec−1, suggesting a substantial and variable, but uncertain net loss of natural carbon from the ocean. Our findings indicate a considerable vulnerability of the ocean carbon sink to climate variability and change. Key Points: - The global ocean storage of anthropogenic carbon grew by 29 ± 3 and 27 ± 3 Pg C dec−1 from 1994 to 2004 and 2004 to 2014, respectively - The change in oceanic storage of anthropogenic carbon relative to the atmospheric CO2 growth decreased by 15 ± 11% from the first to the second decade - This reduction is attributed to a decrease of the ocean buffer capacity and changes in ocean circulation

Description: Flow of dense shelf water provide an efficient mechanism for pumping CO 2 to the deep ocean along the continental shelf slope, particularly around the Antarctic bottom water (AABW) formation areas where much of the global bottom water is formed. However, the contribution of the formation of AABW to sequestering anthropogenic carbon ( C ant ) and its consequences remain unclear. Here, we show prominent transport of C ant (25.0 ± 4.7 Tg C yr −1 ) into the deep ocean (〉2,000 m) in four AABW formation regions around Antarctica based on an integrated observational data set (1974–2018). This maintains a lower C ant in the upper waters than that of other open oceans to sustain a stronger CO 2 uptake capacity (16.9 ± 3.8 Tg C yr −1 ). Nevertheless, the accumulation of C ant can further trigger acidification of AABW at a rate of −0.0006 ± 0.0001 pH unit yr −1 . Our findings elucidate the prominent role of AABW in controlling the Southern Ocean carbon uptake and storage to mitigate climate change, whereas its side effects (e.g., acidification) could also spread to other ocean basins via the global ocean conveyor belt. Plain Language Summary The Southern Ocean is thought to uptake and store a large amount of anthropogenic CO 2 ( C ant ), but little attention has been paid to the Antarctic coastal regions in the south of 60°S, mainly due to the lack of observations. Based on an integrated data set, we discovered the deep penetration of C ant and a visible pattern of relatively high concentration of C ant along the AABW formation pathway, and the concentration of C ant along the shelf‐slope is higher than that of other marginal seas at low‐mid latitudes, implying a highly effective C ant transport in AABW formation areas. We also found strong upper‐layer CO 2 uptake and a significant acidification rate in the deep waters of the Southern Ocean due to the AABW‐driven CO 2 transport, which is 3 times faster than those in other deep oceans. It is therefore crucial to understand how the Antarctic shelf regions affect the global carbon cycle through the uptake and transport of anthropogenic CO 2 , which also drives acidification in the other ocean basins. Key Points We show evidence for the accumulation of C ant along the Antarctic shelf‐slope into the deep ocean The process of AABW formation drives C ant downward transport at 25.0 ± 4.7 Tg C yr −1 , sustaining the CO 2 uptake in the surface ocean This further triggers acidification of AABW at a rate of −0.0006 ± 0.0001 pH unit yr −1 , which is faster than in other deep oceans

Description: We use a 30-year time series (1986–2016) of dichlorodifluoromethane (CFC-12) concentrations with a refined transit time distribution (TTD) method, to estimate the temporal variation of anthropogenic carbon (Cant) in the Central Labrador Sea. We determined that the saturation of CFC-12 and sulfur hexafluroide (SF6) in newly-formed Labrador Sea Water had departed significantly from 100% and varied systematically with time. Multiple linear regression of the time-varying saturation, with the tracer's atmospheric growth rate and the wintertime mixed layer depth as independent variables, allowed reconstruction of the saturation history of CFC-12 and SF6 in wintertime surface waters, which was implemented in the TTD method. Use of the time-varying saturation for CFC-12 gave Cant concentrations ∼7 μmol kg−1 larger than estimates obtained assuming a constant saturation of 100%. The resulting Cant column inventories were ∼20% larger and displayed lower interannual variability compared to conventional TTD-based estimates. The column inventory of Cant increased at an average rate of 1.8 mol m−2 y−1 over the 30-year period. However, the accumulation rate of Cant was higher than this average in the early 1990s and since 2013, whereas inventories remained almost unchanged between 2003 and 2012. The variation in the Cant accumulation rate is shown to be linked to temporal variability in the relative layer thickness of the annually ventilated Labrador Sea Water and the underlying Deep Intermediate Water. The non-steady Cant accumulation highlights the importance of sampling frequency, especially in regions of variable deep mixing and high carbon inventories, and potential misinterpretation of Cant dynamics