Description: The Ocean Model Intercomparison Project (OMIP) focuses on the physics and biogeochemistry of the ocean component of Earth system models participating in the sixth phase of the Coupled Model Intercomparison Project (CMIP6). OMIP aims to provide standard protocols and diagnostics for ocean models, while offering a forum to promote their common assessment and improvement. It also offers to compare solutions of the same ocean models when forced with reanalysis data (OMIP simulations) vs. when integrated within fully coupled Earth system models (CMIP6). Here we detail simulation protocols and diagnostics for OMIP's biogeochemical and inert chemical tracers. These passive-tracer simulations will be coupled to ocean circulation models, initialized with observational data or output from a model spin-up, and forced by repeating the 1948–2009 surface fluxes of heat, fresh water, and momentum. These so-called OMIP-BGC simulations include three inert chemical tracers (CFC-11, CFC-12, SF6) and biogeochemical tracers (e.g., dissolved inorganic carbon, carbon isotopes, alkalinity, nutrients, and oxygen). Modelers will use their preferred prognostic BGC model but should follow common guidelines for gas exchange and carbonate chemistry. Simulations include both natural and total carbon tracers. The required forced simulation (omip1) will be initialized with gridded observational climatologies. An optional forced simulation (omip1-spunup) will be initialized instead with BGC fields from a long model spin-up, preferably for 2000 years or more, and forced by repeating the same 62-year meteorological forcing. That optional run will also include abiotic tracers of total dissolved inorganic carbon and radiocarbon, CTabio and 14CTabio, to assess deep-ocean ventilation and distinguish the role of physics vs. biology. These simulations will be forced by observed atmospheric histories of the three inert gases and CO2 as well as carbon isotope ratios of CO2. OMIP-BGC simulation protocols are founded on those from previous phases of the Ocean Carbon-Cycle Model Intercomparison Project. They have been merged and updated to reflect improvements concerning gas exchange, carbonate chemistry, and new data for initial conditions and atmospheric gas histories. Code is provided to facilitate their implementation.

Description: Developing enduring capacity to monitor ocean life requires investing in people and their institutions to build infrastructure, ownership, and long-term support networks. International initiatives can enhance access to scientific data, tools and methodologies, and develop local expertise to use them, but without ongoing engagement may fail to have lasting benefit. Linking capacity development and technology transfer to sustained ocean monitoring is a win-win proposition. Trained local experts will benefit from joining global communities of experts who are building the comprehensive Global Ocean Observing System (GOOS). This two-way exchange will benefit scientists and policy makers in developing and developed countries. The first step toward the GOOS is complete: identification of an initial set of biological Essential Ocean Variables (EOVs) that incorporate the Group on Earth Observations (GEO) Essential Biological Variables (EBVs), and link to the physical and biogeochemical EOVs. EOVs provide a globally consistent approach to monitoring where the costs of monitoring oceans can be shared and where capacity and expertise can be transferred globally. Integrating monitoring with existing international reporting and policy development connects ocean observations with agreements underlying many countries' commitments and obligations, including under SDG 14, thus catalyzing progress toward sustained use of the ocean. Combining scientific expertise with international capacity development initiatives can help meet the need of developing countries to engage in the agreed United Nations (UN) initiatives including new negotiations for the conservation and sustainable use of marine biological diversity of areas beyond national jurisdiction, and the needs of the global community to understand how the ocean is changing.

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: Iron (Fe) is an essential micronutrient for marine microbial organisms, and low supply controls productivity in large parts of the world’s ocean. The high latitude North Atlantic is seasonally Fe limited, but Fe distributions and source strengths are poorly constrained. Surface ocean dissolved Fe (DFe) concentrations were low in the study region (〈0.1 nM) in summer 2010, with significant perturbations during spring 2010 in the Iceland Basin as a result of an eruption of the Eyjafjallajökull volcano (up to 2.5 nM DFe near Iceland) with biogeochemical consequences. Deep water concentrations in the vicinity of the Reykjanes Ridge system were influenced by pronounced sediment resuspension, with indications for additional inputs by hydrothermal vents, with subsequent lateral transport of Fe and manganese plumes of up to 250–300 km. Particulate Fe formed the dominant pool, as evidenced by 4–17 fold higher total dissolvable Fe compared with DFe concentrations, and a dynamic exchange between the fractions appeared to buffer deep water DFe. Here we show that Fe supply associated with deep winter mixing (up to 103 nmol m−2 d−1) was at least ca. 4–10 times higher than atmospheric deposition, diffusive fluxes at the base of the summer mixed layer, and horizontal surface ocean fluxes.

Description: Ocean ventilation is the integrated effect of various processes that exchange surface properties with the ocean interior and is essential for oxygen supply, storage of anthropogenic carbon and the heat budget of the ocean, for instance. Current observational methods utilise transient tracers, e.g. tritium, SF6, CFCs and 14C. However, their dating ranges are not ideal to resolve the centennial-dynamics of the deep ocean, a gap filled by the noble gas isotope 39Ar with a half-life of 269 years. Its broad application has been hindered by its very low abundance, requiring 1000 L of water for dating. Here we show successful 39Ar dating with 5 L of water based on the atom-optical technique Atom Trap Trace Analysis. Our data reveal previously not quantifiable ventilation patterns in the Tropical Atlantic, where we find that advection is more important for the ventilation of the intermediate depth range than previously assumed. Now, the demonstrated analytical capabilities allow for a global collection of 39Ar data, which will have significant impact on our ability to quantify ocean ventilation.

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: The Southern Ocean is the most important area of anthropogenic carbon (Cant) uptake in the world ocean, only rivalled in importance by the North Atlantic Ocean. Significant variability on decadal time-scales in the uptake of Cant in the Southern Ocean has been observed and modelled, likely with consequences for the interior ocean storage of Cant in the region, and implications for the global carbon budget. Here we use eight cruises between 1973 and 2012 to assess decadal variability in Cant storage rates in the southeast Atlantic sector of the Southern Ocean. For this we employed the extended multiple linear regression (eMLR) method. We relate variability in DIC (dissolved inorganic carbon) storage, which is assumed to equal anthropogenic carbon storage, to changes in ventilation as observed from repeat measurements of transient tracers. Within the Antarctic Intermediate Water (AAIW) layer, which is the dominant transport conduit for Cant into the interior ocean, moderate Cant storage rates were found without any clear temporal trend. In Subantarctic Mode Water (SAMW), a less dense water mass found north of the Subantarctic Front and above AAIW, high storage rates of Cant were observed up to about 2005 but lower rates in more recent times. The transient tracer data suggest a significant speed-up of ventilation in the summer warmed upper part of AAIW between 1998 and 2012, which is consistent with the high storage rate of Cant. A shift of more northern Cant storage to more southern storage in near surface waters was detected in the early 2000s. Beneath the AAIW the eMLR method as applied here did not detect significant storage of Cant. However, the presence of the transient tracer CFC-12 all through the water column suggests that some Cant should be present, but at concentrations not reliably quantifiable. The observed temporal variability in the interior ocean seems at a first glance to be out of phase with observed surface ocean Cant fluxes, but this can be explained by the time delay for the surface ocean signal to manifest itself in the interior of the ocean.

Description: Ocean observations carried out in the framework of the Collaborative Research Center 754 (SFB 754) "Climate-Biogeochemistry Interactions in the Tropical Ocean" are used to study (1) the structure of tropical oxygen minimum zones (OMZs), (2) the processes that contribute to the oxygen budget, and (3) long-term changes in the oxygen distribution. The OMZ of the eastern tropical North Atlantic (ETNA), located between the well-ventilated subtropical gyre and the equatorial oxygen maximum, is composed of a deep OMZ at about 400 m depth with its core region centred at about 20° W, 10° N and a shallow OMZ at about 100 m depth with lowest oxygen concentrations in proximity to the coastal upwelling region off Mauritania and Senegal. The oxygen budget of the deep OMZ is given by oxygen consumption mainly balanced by the oxygen supply due to meridional eddy fluxes (about 60%) and vertical mixing (about 20%, locally up to 30%). Advection by zonal jets is crucial for the establishment of the equatorial oxygen maximum. In the latitude range of the deep OMZ, it dominates the oxygen supply in the upper 300 to 400 m and generates the intermediate oxygen maximum between deep and shallow OMZs. Water mass ages from transient tracers indicate substantially older water masses in the core of the deep OMZ (about 120–180 years) compared to regions north and south of it. The deoxygenation of the ETNA OMZ during recent decades suggests a substantial imbalance in the oxygen budget: about 10% of the oxygen consumption during that period was not balanced by ventilation. Long-term oxygen observations show variability on interannual, decadal and multidecadal time scales that can partly be attributed to circulation changes. In comparison to the ETNA OMZ the eastern tropical South Pacific OMZ shows a similar structure including an equatorial oxygen maximum driven by zonal advection, but overall much lower oxygen concentrations approaching zero in extended regions. As the shape of the OMZs is set by ocean circulation, the widespread misrepresentation of the intermediate circulation in ocean circulation models substantially contributes to their oxygen bias, which might have significant impacts on predictions of future oxygen levels.

Description: Currently available transient tracers have different application ranges that are defined by their temporal input (chronological transient tracers) or their decay rate (radioactive transient tracers). Transient tracers range from tracers for highly ventilated water masses such as sulfur hexafluoride (SF6) through tritium (3H) and chlorofluorocarbons (CFCs) up to tracers for less ventilated deep ocean basins such as argon-39 (39Ar) and radiocarbon (14C). In this context, highly ventilated water masses are defined as water masses that have been in contact with the atmosphere during the last decade. Transient tracers can be used to empirically constrain the transit time distribution (TTD), which can often be approximated with an inverse Gaussian (IG) distribution. The IG-TTD provides information about ventilation and the advective/diffusive characteristics of a water parcel. Here we provide an overview of commonly used transient tracer couples and the corresponding application range of the IG-TTD by using the new concept of validity areas. CFC-12, CFC-11 and SF6 data from three different cruises in the South Atlantic Ocean and Southern Ocean as well as 39Ar data from the 1980s and early 1990s in the eastern Atlantic Ocean and the Weddell Sea are used to demonstrate this method. We found that the IG-TTD can be constrained along the Greenwich Meridian south to 46° S, which corresponds to the Subantarctic Front (SAF) denoting the application limit. The Antarctic Intermediate Water (AAIW) describes the limiting water layer in the vertical. Conspicuous high or lower ratios between the advective and diffusive components describe the transition between the validity area and the application limit of the IG-TTD model rather than describing the physical properties of the water parcel. The combination of 39Ar and CFC data places constraints on the IG-TTD in the deep water north of the SAF, but not beyond this limit.