The coastal ocean contributes to regulating atmospheric greenhouse gas concentrations by taking up carbon dioxide (CO2) and releasing nitrous oxide (N2O) and methane (CH4). Major advances have improved our understanding of the coastal air-sea exchanges of these three gasses since the first phase of the Regional Carbon Cycle Assessment and Processes (RECCAP in 2013), but a comprehensive view that integrates the three gasses at the global scale is still lacking. In this second phase (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 ~60% larger in models (-0.72 vs. -0.44 PgC/yr, 1998-2018, coastal ocean 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 global coastal ocean is a major source of N2O (+0.70 PgCO2-e /yr in observational product and +0.54 PgCO2-e /yr in model median) and of CH4 (+0.21 PgCO2-e /yr in observational product), which offsets a substantial proportion of the net radiative effect of coastal \co uptake (35-58% in CO2-equivalents). Data products and models need improvement to better resolve the spatio-temporal variability and long term trends in CO2, N2O and CH4 in the global coastal ocean.

Due to the complex physical and biogeochemical conditions, the adjacent South Yellow Sea (SYS) and East China Sea (ECS) are ideal sites for studying different carbonate characteristics in marginal seas. The distributions of carbonate system parameters were investigated in this region in early spring and summer. Overall, dissolved inorganic carbon (DIC) and alkalinity concentrations in the SYS were higher than those in the ECS due to the Yellow River runoff which was featured with intensive carbonate weathering and erosion. Low DIC, alkalinity and high pH values were observed in the Zhe-Min Coastal Current with intensive primary production in spring caused by the Changjiang River and Taiwan Warm Current. Temperature and biological activities were the primary drivers in controlling the partial pressure of CO2 (pCO2) variability in the SYS, whereas temperature was the only dominant factor in the outer shelf of the ECS, which was heavily impacted by the Kuroshio Current. The pCO2 dynamics was controlled by primary production and physical mixing in the Changjiang River plume and the inner and middle shelves of the ECS, due to the influence of the Changjiang River with high nutrient supply. Overall, strong CO2 sinks (-4.11 ± 5.28 mmol m-2d-1) turned into weak sources (0.88 ± 5.09 mmol m-2d-1) in the entire study area from spring to summer. Specifically, the SYS and ECS offshore waters changed from CO2 sinks in spring to sources in summer, while the Changjiang River plume always served as a CO2 sink.

Year of emergence (YoE) is the year when an environment and the organisms within begin to experience significant different conditions (two times of natural variability) from the pre-industrial conditions (~1770 C.E.). This study calculates the global surface ocean YoEs for pH, partial pressure of CO(CO) and aragonite saturation (Ω) from a recent calculated surface ocean carbonate chemistry data product. The data product is calculated from the Surface Ocean CO Atlas version 6 (SOCATv6) with modeled CO changes in the global surface ocean from the ESM2M model. We find that CO, pH and Ω generally emerged from preindustrial conditions in the open ocean by the year 1950, while these properties have still not yet emerged along many ocean margins. We also find that Ω had a significantly delayed YoE compared to pH and CO. The delayed YoE for Ω is caused by its lasting sensitivity to temperature variability, which increases the natural variability experienced by organisms, and a partial cancellation of the long term acidification trend by the global warming. Together, YoEs presented here highlight that there are hotspots (open ocean) and coldspots (ocean margins that were impacted by boundary currents) for the emergence of anthropogenic signals. Continuous data collection and synthesis are needed to further examine the impact of ocean acidification on ecosystem health.

A key to better constraining estimates of the ocean sink for fossil fuel emissions of carbon dioxide is reducing uncertainties in coastal carbon fluxes. A contributing factor in uncertainties in coastal carbon fluxes stems from the under sampling of seasonality and spatial heterogeneity. Our objectives were to i) assess satellite-based approaches that would expand the spatial and temporal coverage of the surface ocean pCO2 and sea-air CO2 flux for the northern Gulf of Mexico, and ii) investigate the seasonal and interannual variations in CO2 dynamics and possible environmental drivers. Regression tree analysis was effective in directly relating surface ocean pCO2 to satellite-retrieved (MODIS Aqua) products including chlorophyll, sea surface temperature, and dissolved/detrital absorption. Satellite-based assessments of sea surface pCO2 were made spanning the period from 2006-2010 and were used in conjunction with estimates of wind fields and atmospheric pCO2 to produce regional-scale estimates of air-sea fluxes. Seasonality was evident in air-sea fluxes of CO2, with an estimated annual average CO2 flux for the study region of -4.3 + 1.1 Tg C y-1, confirming prior findings that the Gulf of Mexico was a net CO2 sink. Interannual variability in fluxes was related to Mississippi River dissolved inorganic nitrogen inputs, an indication that human- and climate-related changes in river exports will impact coastal carbon budgets. This is the first multi-year assessment of pCO2 and air-sea flux of CO2 using satellite-derived environmental data for the northern Gulf of Mexico.