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The Washington State Department of Ecology conducted a large-scale ocean acidification (OA) study in greater Puget Sound to: (1) produce a marine carbon dioxide (CO2) system dataset capable of distinguishing between long-term anthropogenic changes and natural variability, (2) characterize how rivers and freshwater drive OA conditions in the region, and (3) understand the relative influence of cumulative anthropogenic forcing on regional OA conditions. Marine CO2 system data were collected monthly at 20 stations between October 2018 and February 2020. While additional data are still needed, the climate-level data collected thus far have uncovered novel insights into spatiotemporal distributions of and variability in the regional marine CO2 system, especially at low salinities in shallow, river-forced shelf regions. The data provide a strong foundation with which to continue monitoring OA conditions across the region. More importantly, this work represents the first successful long-term OA monitoring program undertaken at the state-level by a regulatory agency. Therefore, we offer the work described herein as a blueprint to help state and local scientists and environmental and natural resource managers develop, implement, and conduct long-term OA monitoring programs and studies in their own contexts and jurisdictions. [ABSTRACT FROM AUTHOR]

Fingerprinting ocean acidification (OA) in US West Coast waters is extremely challenging due to the large magnitude of natural carbonate chemistry variations common to these regions. Additionally, quantifying a change requires information about the initial conditions, which is not readily available in most coastal systems. In an effort to address this issue, we have collated high-quality publicly available data to characterize the modern seasonal carbonate chemistry variability in marine surface waters of the US Pacific Northwest. Underway ship data from version 4 of the Surface Ocean CO2 Atlas, discrete observations from various sampling platforms, and sustained measurements from regional moorings were incorporated to provide ~ 100 000 inorganic carbon observations from which modern seasonal cycles were estimated. Underway ship and discrete observations were merged and gridded to a 0.1° x 0.1° scale. Eight unique regions were identified and seasonal cycles from grid cells within each region were averaged. Data from nine surface moorings were also compiled and used to develop robust estimates of mean seasonal cycles for comparison with the eight regions. This manuscript describes our methodology and the resulting mean seasonal cycles for multiple OA metrics in an effort to provide a largescale environmental context for ongoing research, adaptation, and management efforts throughout the US Pacific Northwest. Major findings include the identification of unique chemical characteristics across the study domain. There is a clear increase in the ratio of dissolved inorganic carbon (DIC) to total alkalinity (TA) and in the seasonal cycle amplitude of carbonate system parameters when moving from the open ocean North Pacific into the Salish Sea. Due to the logarithmic nature of the pH scale (pHD=-log10[HC], where [HC] is the hydrogen ion concentration), lower annual mean pH values (associated with elevated DIC V TA ratios) coupled with larger magnitude seasonal pH cycles results in seasonal [HC] ranges that are ~27 times larger in Hood Canal than in the neighboring North Pacific open ocean. Organisms living in the Salish Sea are thus exposed to much larger seasonal acidity changes than those living in nearby open ocean waters. Additionally, our findings suggest that lower buffering capacities in the Salish Sea make these waters less efficient at absorbing anthropogenic carbon than open ocean waters at the same latitude. All data used in this analysis are publically available at the following websites: - Surface Ocean CO2 Atlas version 4 coastal data, https://doi.pangaea.de/10.1594/PANGAEA. 866856 (Bakker et al., 2016a); - National Oceanic and Atmospheric Administration (NOAA) West Coast Ocean Acidification cruise data, https://doi.org/10.3334/CDIAC/otg.CLIVAR_NACP_West_Coast_Cruise_2007 (Feely and Sabine, 2013); https://doi.org/10.7289/V5JQ0XZ1 (Feely et al., 2015b); https://data.nodc.noaa.gov/cgi-bin/iso?id=gov.noaa.nodc:0157445 (Feely et al., 2016a); https://doi.org/10.7289/V5C53HXP (Feely et al., 2015a); - University of Washington (UW) and Washington Ocean Acidification Center cruise data, https://doi.org/10. 5281/zenodo.1184657 (Fassbender et al., 2018); - Washington State Department of Ecology seaplane data, https://doi.org/10.5281/zenodo.1184657 (Fassbender et al., 2018); - NOAA Moored Autonomous pCO2 (MAPCO2) buoy data, https://doi.org/10.3334/CDIAC/OTG.TSM_ LAPUSH_125W_48N (Sutton et al., 2012); https://doi.org/10.3334/CDIAC/OTG.TSM_WA_125W_ 47N (Sutton et al., 2013); https://doi.org/10.3334/CDIAC/OTG.TSM_DABOB_122W_478N (Sutton et al., 2014a); https://doi.org/10.3334/CDIAC/OTG.TSM_TWANOH_123W_47N (Sutton et al., 2016a); - UW Oceanic Remote Chemical/Optical Analyzer buoy data, https://doi.org/10.5281/zenodo.1184657 (Fassbender et al., 2018); - NOAA Pacific Coast Ocean Observing System cruise data, https://doi.org/10.5281/zenodo. 1184657 (Fassbender et al., 2018). [ABSTRACT FROM AUTHOR]

Fingerprinting ocean acidification (OA) in U.S. West Coast waters is extremely challenging due to the large magnitude of natural carbonate chemistry variations common to these regions. Additionally, quantifying a change requires information about the initial conditions, which is not readily available in most coastal systems. In an effort to address this issue, we have collated high-quality, publicly-available data to characterize the modern seasonal carbonate chemistry variability in marine surface waters of the Pacific Northwest. Underway ship data from Version 4 of the Surface Ocean CO2 Atlas, discrete observations from various sampling platforms, and sustained measurements from regional moorings were incorporated to provide ~100,000 inorganic carbon observations from which modern seasonal cycles were estimated. Underway ship and discrete observations were merged and gridded to a 0.1°×0.1° scale. Eight unique regions were identified and seasonal cycles from grid cells within each region were averaged. Data from nine surface moorings were also compiled and used to develop robust estimates of mean seasonal cycles for comparison with the eight regions. This manuscript describes our methodology and the resulting mean seasonal cycles for multiple OA metrics in an effort to provide large-scale, environmental context for ongoing research, adaptation, and management efforts throughout the Pacific Northwest. Major findings include the identification of unique chemical characteristics across the study domain. There is a clear increase in the ratio of dissolved inorganic carbon (DIC) to total alkalinity (TA) and in the seasonal cycle amplitude of carbonate system parameters when moving from the open ocean North Pacific into the Salish Sea. Due to the logarithmic nature of the pH scale (pH=−log10[H+], where [H+] is the hydrogen ion concentration), lower annual mean pH values (associated with elevated DIC:TA) coupled with larger magnitude seasonal pH cycles results in seasonal [H+] ranges that are ~27 times larger in Hood Canal than in the neighboring North Pacific open ocean. Organisms living in the Salish Sea are thus exposed to much larger seasonal acidity changes than those living in nearby open ocean waters. Additionally, our findings suggest that lower buffering capacities in the Salish Sea make these waters less efficient at absorbing anthropogenic carbon than open ocean waters at the same latitude. [ABSTRACT FROM AUTHOR]