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Abstract Uptake of anthropogenic carbon dioxide from the atmosphere by the surface ocean is leading to global ocean acidification, but regional variations in ocean circulation and mixing can dampen or accelerate apparent acidification rates. Here we use a regional ocean model simulation for the years 1980 to 2013 and observational data to investigate how ocean fluctuations impact acidification rates in surface waters of the Gulf of Alaska. We find that large-scale atmospheric forcing influenced local winds and upwelling strength, which in turn affected ocean acidification rate. Specifically, variability in local wind stress curl depressed sea surface height in the subpolar gyre over decade-long intervals, which increased upwelling of nitrate- and dissolved inorganic carbon-rich waters and enhanced apparent ocean acidification rates. We define this sea surface height variability as the Northern Gulf of Alaska Oscillation and suggest that it can cause extreme acidification events that are detrimental to ecosystem health and fisheries. 

Abstract. The coastal ecosystem of the Gulf of Alaska (GOA) is especially vulnerable to the effects of ocean acidification and climate change. Detection of these long-term trends requires a good understanding of the system’s natural state. The GOA is a highly dynamic system that exhibits large inorganic carbon variability on subseasonal to interannual timescales. This variability is poorly understood due to the lack of observations in this expansive and remote region. We developed a new model setup for the GOA that couples the three-dimensional Regional Oceanic Model System (ROMS) and the Carbon, Ocean Biogeochemistry and Lower Trophic (COBALT) ecosystem model. To improve our conceptual understanding of the system, we conducted a hindcast simulation from 1980 to 2013. The model was explicitly forced with temporally and spatially varying coastal freshwater discharges from a high-resolution terrestrial hydrological model, thereby affecting salinity, alkalinity, dissolved inorganic carbon, and nutrient concentrations. This represents a substantial improvement over previous GOA modeling attempts. Here, we evaluate the model on seasonal to interannual timescales using the best available inorganic carbon observations. The model was particularly successful in reproducing observed aragonite oversaturation and undersaturation of near-bottom water in May and September, respectively. The largest deficiency in the model is its inability to adequately simulate springtime surface inorganic carbon chemistry, as it overestimates surface dissolved inorganic carbon, which translates into an underestimation of the surface aragonite saturation state at this time. We also use the model to describe the seasonal cycle and drivers of inorganic carbon parameters along the Seward Line transect in under-sampled months. Model output suggests that the majority of the near-bottom water along the Seward Line is seasonally undersaturated with respect to aragonite between June and January, as a result of upwelling and remineralization. Such an extensive period of reoccurring aragonite undersaturation may be harmful to ocean acidification-sensitive organisms. Furthermore, the influence of freshwater not only decreases the aragonite saturation state in coastal surface waters in summer and fall, but it simultaneously decreases the surface partial pressure of carbon dioxide (pCO2), thereby decoupling the aragonite saturation state from pCO2. The full seasonal cycle and geographic extent of the GOA region is under-sampled, and our model results give new and important insights for months of the year and areas that lack in situ inorganic carbon observations. 

Abstract For the first time the annual carbon budget on the West Antarctic Peninsula shelf was studied with continuously measured CO₂system parameters (pH andpCO₂) from a subsurface mooring. The temporal evolution of the mixed layer dissolved inorganic carbon (DIC) is investigated via a mass balance. The annual mixed layer DIC inventory change was 1.1 ± 0.4 mol m⁻² yr⁻¹, which was mainly regulated by biological drawdown (−2.8 ± 2.4 mol m⁻² yr⁻¹), diapycnal eddy diffusion (2.6 ± 1.3 mol m⁻² yr⁻¹), entrainment/detrainment (0.9 ± 0.4 mol m⁻² yr⁻¹), and air‐water gas exchange (0.4 ± 2.1 mol m⁻² yr⁻¹). Significant carbon drawdown was observed in the spring and summer, which was replenished by the physical processes mentioned above. These observations suggest this area is an annual atmosphere CO₂sink with a mixed layer net community production of 2.8 ± 2.4 mol m⁻² yr⁻¹. These results highlight the significant seasonality in the DIC mass balance and the necessity of year‐round continuous observations for robust assessments of biogeochemical cycling in this region.