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The global ocean takes up nearly a quarter of anthropogenic CO 2 emissions annually, but the variability in this uptake at regional scales remains poorly understood. Here we use a neural network approach to interpolate sparse observations, creating a monthly gridded seawater partial pressure of CO 2 (p CO 2) data product from January 1998 to December 2019, at 1/12 ∘ × 1/12 ∘ spatial resolution, in the northeast Pacific open ocean, a net sink region. The data product (ANN-NEP; NCEI Accession 0277836) was created from p CO 2 observations within the 2021 version of the Surface Ocean CO 2 Atlas (SOCAT) and a range of predictor variables acting as proxies for processes affecting p CO 2 to create nonlinear relationships to interpolate observations at a spatial resolution 4 times greater than leading global products and with better overall performance. In moving to a higher resolution, we show that the internal division of training data is the most important parameter for reducing overfitting. Using our p CO 2 product, wind speed, and atmospheric CO 2 , we evaluate air–sea CO 2 flux variability. On sub-decadal to decadal timescales, we find that the upwelling strength of the subpolar Alaskan Gyre, driven by large-scale atmospheric forcing, acts as the primary control on air–sea CO 2 flux variability (r2=0.93 , p<0.01). In the northern part of our study region, divergence from atmospheric CO 2 is enhanced by increased local wind stress curl, enhancing upwelling and entrainment of naturally CO 2 -rich subsurface waters, leading to decade-long intervals of strong winter outgassing. During recent Pacific marine heat waves from 2013 on, we find enhanced atmospheric CO 2 uptake (by as much as 45 %) due to limited wintertime entrainment. Our product estimates long-term surface ocean p CO 2 increase at a rate below the atmospheric trend (1.4 ± 0.1 µ atm yr -1) with the slowest increase in the center of the subpolar gyre where there is strong interaction with subsurface waters. This mismatch suggests the northeast Pacific Ocean sink for atmospheric CO 2 may be increasing. [ABSTRACT FROM AUTHOR]

Abstract: Oceanographic surveys of surface water hydrography, pCO2, biological O2 saturation (ΔO2/Ar) and dimethylsulfide (DMS) were conducted around Vancouver Island, B.C. during late spring of 2007 and 2010. Winter El Niño conditions during early 2010 resulted in strong downwelling and decreased sub-surface nutrient inventories relative to 2007, while reduced Fraser River input, high wind speeds and greater cloud cover led to relatively weak vertical stratification and decreased sea surface irradiance during the 2010 survey. Phytoplankton biomass (Chla) was significantly higher along the west coast of Vancouver Island (WCVI) during late May 2007, and we observed a strong biological imprint on surface gas distributions during this survey, with biologically induced O2 saturation in excess of 40%. Minimum pCO2 along the WCVI was 100ppm during the 2007 survey, and this region served as a moderate CO2 sink at the time of our sampling (mean sea-air flux of -3.2mmolCO2 m−2 d−1). By comparison, both pCO2 and ΔO2/Ar were much closer to atmospheric equilibrium during our 2010 survey. Despite these lower sea-air gradients, high wind speeds led to a significantly larger CO2 sink (13.4mmolm−2 d−1) during the 2010 survey, and a greater uncoupling of ΔO2/Ar and pCO2 through differential gas exchange. Relative to the WCVI, pCO2 and ΔO2/Ar distributions showed smaller differences among cruises along the east coast of Vancouver Island (ECVI), where surface water properties were largely driven by physical circulation. Nonetheless, we did observe lower pCO2 and higher ΔO2/Ar in the Strait of Georgia during the 2010 survey, possibly due to a wind-driven mixing event which may have stimulated local primary productivity. DMS concentrations exhibited large ranges and significant small-scale spatial variability for both cruises, but mean DMS concentrations were more than three-fold higher along the WCVI during late May 2007. Higher wind speeds in late May 2010 led to greater DMS fluxes during our 2010 survey (10 vs. 5μmolm−2 d−1 for 2010 and 2007, respectively) despite lower sea-air concentration gradients. For both cruises, about 40% of the variability in surface water DMS concentrations was explained by Chla/mixed layer depth ratios when data were binned to a spatial resolution of 0.25°. Based on our results, we discuss the potential linkages between regional climate variability and surface gases in coastal B.C. waters. [Copyright &y& Elsevier]

Abstract: Sea-air carbon dioxide (CO2) fluxes have been analyzed from recently-collected winter, summer and autumn surface ocean CO2 partial pressure (pCO2) data spanning a large portion of the western Canadian coastal ocean, and historical underway pCO2 measurements from the southwest Vancouver Island shelf and the Strait of Juan de Fuca. Sea-air CO2 fluxes from the recent data for specific subregions of the coastal ocean, selected based on geography or bathymetry, were used to make seasonal area-specific estimates of CO2 exchange. These show significant differences between subregions, which have important consequences for estimating seasonal area-weighted fluxes on the margin. Climatologies of sea-air CO2 flux were calculated from the historical data using two approaches: One based on fluxes calculated from temporally-averaged values of sea-air pCO2 differences, solubility and gas transfer velocities, and the other from temporally-averaged instantaneous flux estimates. Seasonal flux estimates from our recently-collected data are consistent with the climatological estimates, in that both show stronger outgassing of CO2 in autumn relative to winter, and both reveal straits as important atmospheric CO2 source regions. Taken together, both analyses of recent and historical data suggest that the transition seasons (spring and autumn) contain the largest (positive and negative) fluxes because of the coincidence of high gas transfer velocities and large surface seawater disequilibria with the atmosphere. By combining the results from these analyses, and making some assumptions where data are missing, we estimate moderate net annual sea-air CO2 influx in the western Canadian coastal ocean of −6mmolm−2 d−1. [Copyright &y& Elsevier]

The absorption of atmospheric carbon dioxide (CO2) into the ocean lowers the pH of the waters. This so-called ocean acidification could have important consequences for marine ecosystems. To better understand the extent of this ocean acidification in coastal waters, we conducted hydrographic surveys along the continental shelf of western North America from central Canada to northern Mexico. We observed seawater that is undersaturated with respect to aragonite üpwelling onto Large portions of the continental shelf, reaching depths of -.40 to 120 meters along most transect tines and all the way to the surface on one transect off northern California. Although seasonal upwetting of the undersaturated waters onto the shelf is a natural phenomenon in this region, the ocean uptake of anthropogenic CO2 has increased the areal extent of the affected area. [ABSTRACT FROM AUTHOR]