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Abstract The ocean is a major carbon sink and takes up 25%–30% of the anthropogenically emitted CO₂. A state‐of‐the‐art method to quantify this sink are global ocean biogeochemistry models (GOBMs), but their simulated CO₂uptake differs between models and is systematically lower than estimates based on statistical methods using surface oceanpCO₂and interior ocean measurements. Here, we provide an in‐depth evaluation of ocean carbon sink estimates from 1980 to 2018 from a GOBM ensemble. As sources of inter‐model differences and ensemble‐mean biases our study identifies (a) the model setup, such as the length of the spin‐up, the starting date of the simulation, and carbon fluxes from rivers and into sediments, (b) the simulated ocean circulation, such as Atlantic Meridional Overturning Circulation and Southern Ocean mode and intermediate water formation, and (c) the simulated oceanic buffer capacity. Our analysis suggests that a late starting date and biases in the ocean circulation cause a too low anthropogenic CO₂uptake across the GOBM ensemble. Surface ocean biogeochemistry biases might also cause simulated anthropogenic fluxes to be too low, but the current setup prevents a robust assessment. For simulations of the ocean carbon sink, we recommend in the short‐term to (a) start simulations at a common date before the industrialization and the associated atmospheric CO₂increase, (b) conduct a sufficiently long spin‐up such that the GOBMs reach steady‐state, and (c) provide key metrics for circulation, biogeochemistry, and the land‐ocean interface. In the long‐term, we recommend improving the representation of these metrics in the GOBMs. 

Abstract We assess the Southern Ocean CO₂uptake (1985–2018) using data sets gathered in the REgional Carbon Cycle Assessment and Processes Project Phase 2. The Southern Ocean acted as a sink for CO₂with close agreement between simulation results from global ocean biogeochemistry models (GOBMs, 0.75 ± 0.28 PgC yr⁻¹) andpCO₂‐observation‐based products (0.73 ± 0.07 PgC yr⁻¹). This sink is only half that reported by RECCAP1 for the same region and timeframe. The present‐day net uptake is to first order a response to rising atmospheric CO₂, driving large amounts of anthropogenic CO₂(C_ant) into the ocean, thereby overcompensating the loss of natural CO₂to the atmosphere. An apparent knowledge gap is the increase of the sink since 2000, withpCO₂‐products suggesting a growth that is more than twice as strong and uncertain as that of GOBMs (0.26 ± 0.06 and 0.11 ± 0.03 Pg C yr⁻¹ decade⁻¹, respectively). This is despite nearly identicalpCO₂trends in GOBMs andpCO₂‐products when both products are compared only at the locations wherepCO₂was measured. Seasonal analyses revealed agreement in driving processes in winter with uncertainty in the magnitude of outgassing, whereas discrepancies are more fundamental in summer, when GOBMs exhibit difficulties in simulating the effects of the non‐thermal processes of biology and mixing/circulation. Ocean interior accumulation of C_antpoints to an underestimate of C_antuptake and storage in GOBMs. Future work needs to link surface fluxes and interior ocean transport, build long overdue systematic observation networks and push toward better process understanding of drivers of the carbon cycle. 

Abstract. As the largest active carbon reservoir on Earth, the ocean is a cornerstone of the global carbon cycle, playing a pivotal role in modulating ocean health and regulating climate. Understanding these crucial roles requires access to a broad array of data products documenting the changing chemistry of the global ocean as a vast and interconnected system. This review article provides a comprehensive overview of 60 existing ocean carbonate chemistry data products, encompassing compilations of cruise datasets, derived gap-filled data products, model simulations, and compilations thereof. It is intended to help researchers identify and access data products that best align with their research objectives, thereby advancing our understanding of the ocean's evolving carbonate chemistry. 

Abstract This contribution to the RECCAP2 (REgional Carbon Cycle Assessment and Processes) assessment analyzes the processes that determine the global ocean carbon sink, and its trends and variability over the period 1985–2018, using a combination of models and observation‐based products. The mean sea‐air CO₂flux from 1985 to 2018 is −1.6 ± 0.2 PgC yr⁻¹based on an ensemble of reconstructions of the history of sea surface pCO₂(pCO₂products). Models indicate that the dominant component of this flux is the net oceanic uptake of anthropogenic CO₂, which is estimated at −2.1 ± 0.3 PgC yr⁻¹by an ensemble of ocean biogeochemical models, and −2.4 ± 0.1 PgC yr⁻¹by two ocean circulation inverse models. The ocean also degasses about 0.65 ± 0.3 PgC yr⁻¹of terrestrially derived CO₂, but this process is not fully resolved by any of the models used here. From 2001 to 2018, the pCO₂products reconstruct a trend in the ocean carbon sink of −0.61 ± 0.12 PgC yr⁻¹ decade⁻¹, while biogeochemical models and inverse models diagnose an anthropogenic CO₂‐driven trend of −0.34 ± 0.06 and −0.41 ± 0.03 PgC yr⁻¹ decade⁻¹, respectively. This implies a climate‐forced acceleration of the ocean carbon sink in recent decades, but there are still large uncertainties on the magnitude and cause of this trend. The interannual to decadal variability of the global carbon sink is mainly driven by climate variability, with the climate‐driven variability exceeding the CO₂‐forced variability by 2–3 times. These results suggest that anthropogenic CO₂dominates the ocean CO₂sink, while climate‐driven variability is potentially large but highly uncertain and not consistently captured across different methods.