Description: The Apparent Oxygen Utilisation (AOU) is a classical measure of the amount of oxygen respired in the ocean's interior. We show that AOU systematically overestimates True Oxygen Utilisation (TOU) in 6 coupled circulation-biogeochemical ocean models. This is due to atmosphere–ocean oxygen disequilibria in the subduction regions, consistent with previous work. We develop a simple, new, observationally-based approach which we call Evaluated Oxygen Utilisation (EOU). In this approach, we take into account the impact of the upper ocean oxygen disequilibria into the interior, considering that transport takes place predominantly along isopycnal surfaces. The EOU approximates the TOU with less than half of the bias of AOU in all 6 models despite large differences in the physical and biological components of the models. Applying the EOU approach to a global observational dataset yields an oxygen consumption rate 25% lower than that derived from AOU-based estimates, for a given ventilation rate.

Description: Phosphate distributions simulated by seven state-of-the-art biogeochemical ocean circulation models are evaluated against observations of global ocean nutrient distributions. The biogeochemical models exhibit different structural complexities, ranging from simple nutrient-restoring to multi-nutrient NPZD type models. We evaluate the simulations using the observed volume distribution of phosphate. The errors in these simulated volume class distributions are significantly larger when preformed phosphate (or regenerated phosphate) rather than total phosphate is considered. Our analysis reveals that models can achieve similarly good fits to observed total phosphate distributions for a very different partitioning into preformed and regenerated nutrient components. This has implications for the strength and potential climate sensitivity of the simulated biological carbon pump. We suggest complementing the use of total nutrient distributions for assessing model skill by an evaluation of the respective preformed and regenerated nutrient components.

Description: The abundance and size distribution of marine particles control a range of biogeochemical and ecological processes in the ocean, including carbon sequestration. These quantities are the result of complex physical-biological interactions that are difficult to observe, and their spatial and temporal patterns remain uncertain. Here, we present a novel analysis of particle size distributions (PSDs) from a global compilation of in situ Underwater Vision Profiler 5 (UVP5) optical measurements. Using a machine learning algorithm, we extrapolate sparse UVP5 observations to the global ocean from well-sampled oceanographic variables. We reconstruct global maps of PSD parameters (biovolume [BV] and slope) for particles at the base of the euphotic zone. These reconstructions reveal consistent global patterns, with high chlorophyll regions generally characterized by high particle BV and flatter PSD slope, that is, a high relative abundance of large versus small particles. The resulting negative correlations between particle BV and slope further suggests synergistic effects on size-dependent processes such as sinking particle fluxes. Our approach and estimates provide a baseline for an improved understanding of particle cycles in the ocean, and pave the way to global, three-dimensional reconstructions of PSD and sinking particle fluxes from the growing body of UVP5 observations.

Description: Export of sinking particles from the surface ocean is critical for carbon sequestration and to provide energy to the deep biosphere. The magnitude and spatial patterns of this export have been estimated in the past by in situ particle flux observations, satellite-based algorithms, and ocean biogeochemical models; however, these estimates remain uncertain. Here, we use a recent machine learning reconstruction of global ocean particle size distributions (PSDs) from Underwater Vision Profiler 5 measurements to estimate carbon fluxes by sinking particles (35 μm–5 mm equivalent spherical diameter) from the surface ocean. We combine global maps of PSD properties with empirical relationships constrained against in situ flux observations to calculate particulate carbon export from the euphotic zone (5.8 ± 0.1 Pg C y−1) and annual maximum mixed layer depths (6.1 ± 0.1 Pg C y−1). The new flux reconstructions suggest a less variable seasonal cycle in the tropical ocean and a more persistent export in the Southern Ocean than previously recognized. Smaller particles (less than 418 μm) contribute most of the flux globally, while larger particles become more important at high latitudes and in tropical upwelling regions. Export from the annual maximum mixed layer exceeds that from the euphotic zone over most of the low-latitude ocean, suggesting shallow particle recycling and net heterotrophy in the deep euphotic zone. These estimates open the way to fully three-dimensional global reconstructions of particle fluxes in the ocean, supported by the growing database of in situ optical observations.

Description: The coastal ocean contributes to regulating atmospheric greenhouse gas concentrations by taking up carbon dioxide (CO2) and releasing nitrous oxide (N2O) and methane (CH4). In this second phase of the Regional Carbon Cycle Assessment and Processes (RECCAP2), we quantify global coastal ocean fluxes of CO2, N2O and CH4 using an ensemble of global gap-filled observation-based products and ocean biogeochemical models. The global coastal ocean is a net sink of CO2 in both observational products and models, but the magnitude of the median net global coastal uptake is similar to 60% larger in models (-0.72 vs. -0.44 PgC year-1, 1998-2018, coastal ocean extending to 300 km offshore or 1,000 m isobath with area of 77 million km2). We attribute most of this model-product difference to the seasonality in sea surface CO2 partial pressure at mid- and high-latitudes, where models simulate stronger winter CO2 uptake. The coastal ocean CO2 sink has increased in the past decades but the available time-resolving observation-based products and models show large discrepancies in the magnitude of this increase. The global coastal ocean is a major source of N2O (+0.70 PgCO2-e year-1 in observational product and +0.54 PgCO2-e year-1 in model median) and CH4 (+0.21 PgCO2-e year-1 in observational product), which offsets a substantial proportion of the coastal CO2 uptake in the net radiative balance (30%-60% in CO2-equivalents), highlighting the importance of considering the three greenhouse gases when examining the influence of the coastal ocean on climate. The coastal ocean regulates greenhouse gases. It acts as a sink of carbon dioxide (CO2) but also releases nitrous oxide (N2O) and methane (CH4) into the atmosphere. This synthesis contributes to the second phase of the Regional Carbon Cycle Assessment and Processes (RECCAP2) and provides a comprehensive view of the coastal air-sea fluxes of these three greenhouse gases at the global scale. We use a multi-faceted approach combining gap-filled observation-based products and ocean biogeochemical models. We show that the global coastal ocean is a net sink of CO2 in both observational products and models, but the coastal uptake of CO2 is similar to 60% larger in models than in observation-based products due to model-product differences in seasonality. The coastal CO2 sink is strengthening but the magnitude of this strengthening is poorly constrained. We also find that the coastal emissions of N2O and CH4 counteract a substantial part of the effect of coastal CO2 uptake in the atmospheric radiative balance (by 30%-60% in CO2-equivalents), highlighting the need to consider these three gases together to understand the influence of the coastal ocean on climate. We synthesize air-sea fluxes of CO2, nitrous oxide and methane in the global coastal ocean using observation-based products and ocean models The coastal ocean CO2 sink is 60% larger in ocean models than in observation-based products due to systematic differences in seasonality Coastal nitrous oxide and methane emissions offset 30%-60% of the CO2 coastal uptake in the net radiative balance