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Abstract Mapped monthly data products of surface ocean acidification indicators from 1998 to 2022 on a 0.25° by 0.25° spatial grid have been developed for eleven U.S. large marine ecosystems (LMEs). The data products were constructed using observations from the Surface Ocean CO₂Atlas, co-located surface ocean properties, and two types of machine learning algorithms: Gaussian mixture models to organize LMEs into clusters of similar environmental variability and random forest regressions (RFRs) that were trained and applied within each cluster to spatiotemporally interpolate the observational data. The data products, called RFR-LMEs, have been averaged into regional timeseries to summarize the status of ocean acidification in U.S. coastal waters, showing a domain-wide carbon dioxide partial pressure increase of 1.4 ± 0.4 μatm yr⁻¹and pH decrease of 0.0014 ± 0.0004 yr⁻¹. RFR-LMEs have been evaluated via comparisons to discrete shipboard data, fixed timeseries, and other mapped surface ocean carbon chemistry data products. Regionally averaged timeseries of RFR-LME indicators are provided online through the NOAA National Marine Ecosystem Status web portal. 

Abstract. The ocean is one of the largest sinks for anthropogenic carbon dioxide (Canth) and its removal of carbon dioxide (CO2) from the atmosphere has been valued at hundreds of billions to trillions of US dollars in climate mitigation annually. The ecosystem impacts caused by planet-wide shifts in ocean chemistry resulting from marine Canth accumulation are an active area of research. For these reasons, we need accessible tools to quantify ocean Canth inventories and distributions and to predict how they might evolve in response to future emissions and mitigation activities. Unfortunately, Canth estimation methods are typically only accessible to trained scientists and modelers with access to significant computational resources. Here, we make modifications to the transit time distribution approach for Canth estimation that render the method more accessible. We also release software (BRCScienceProducts, 2025) called “Tracer-based Rapid Anthropogenic Carbon Estimation version 1” (TRACEv1) that allows users – with one line of code – to obtain Canth and water mass age estimates throughout the global open ocean from user-supplied values of geographic location, pressure, salinity, temperature, and the estimate year. We use this code to generate a data product of global gridded open-ocean Canth distributions (TRACEv1_GGCanth; Carter, 2025) that ranges from the preindustrial era through 2500 under a range of Shared Socioeconomic Pathways (SSPs, or atmospheric CO2 concentration pathways). We estimated the skill of these estimates by reconstructing Canth in models with known distributions of Canth and transient tracers and by conducting perturbation tests. In the model-based reconstruction test, TRACEv1 reproduces the global ocean Canth inventory to within ±10 % in 1980 and 2014. We discuss implications and limitations of the projected Canth distributions and highlight ways that the estimation strategy might be improved. One finding is that the ocean will continue to increase its net Canth inventory at least through 2500 due to deep-ocean ventilation, even with the SSP in which intense mitigation successfully decreases atmospheric Canth by ∼60 % in 2500 relative to the 2024 concentration. A notable limitation of this and similar projections made with TRACEv1 is that ongoing and potential future warming and changing oceanic circulation patterns with climate change are not captured by the method. The data products generated by this research are available as MATLAB code (https://doi.org/10.5281/zenodo.15692788, BRCScienceProducts, 2025) and a spatially and temporally gridded data product (https://doi.org/10.5281/zenodo.15692788, BRCScienceProducts, 2025). 

Abstract The California Current Ecosystem (CCE) is a natural laboratory for studying the chemical and ecological impacts of ocean acidification. Biogeochemical variability in the region is due primarily to wind‐driven near‐shore upwelling of cold waters that are rich in re‐mineralized carbon and poor in oxygen. The coastal regions are exposed to surface waters with increasing concentrations of anthropogenic CO₂(C_anth) from exchanges with the atmosphere and the shoreward transport and mixing of upwelled water. The upwelling drives intense cycling of organic matter that is created through photosynthesis in the surface ocean and degraded through biological respiration in subsurface habitats. We used an extended multiple linear‐regression approach to determine the spatial and temporal concentrations of C_anthand respired carbon (C_bio) in the CCE based on cruise data from 2007, 2011, 2012, 2013, 2016, and 2021. Over the region, the C_anthaccumulation rate increased from 0.8 ± 0.1 μmol kg⁻¹ yr⁻¹in the northern latitudes to 1.1 ± 0.1 μmol kg⁻¹ yr⁻¹further south. The rates decreased to values of about ∼0.3 μmol kg⁻¹ yr⁻¹at depths near 300 m. These accumulation rates at the surface correspond to total pH decreases that averaged about 0.002 yr^‐1; whereas, decreases in aragonite saturation state ranged from 0.006 to 0.011 yr^‐1. The impact of the C_anthuptake was to decrease the amount of oxygen consumption required to cross critical biological thresholds (i.e., calcification, dissolution) for marine calcifiers and are significantly lower in the recent cruises than in the pre‐industrial period because of the addition of C_anth. 

Abstract Seawater carbonate chemistry observations are increasingly necessary to study a broad array of oceanographic challenges such as ocean acidification, carbon inventory tracking, and assessment of marine carbon dioxide removal strategies. The uncertainty in a seawater carbonate chemistry observation comes from unknown random variations and systematic offsets. Here, we estimate the magnitudes of these random and systematic components of uncertainty for the discrete open‐ocean carbonate chemistry measurements in the Global Ocean Data Analysis Project 2022 update (GLODAPv2.2022). We use both an uncertainty propagation approach and a carbonate chemistry measurement “inter‐consistency” approach that quantifies the disagreement between measured carbonate chemistry variables and calculations of the same variables from other carbonate chemistry measurements. Our inter‐consistency analysis reveals that the seawater carbonate chemistry measurement community has collected and released data with a random uncertainty that averages about 1.7 times the uncertainty estimated by propagating the desired “climate‐quality” random uncertainties. However, we obtain differing random uncertainty estimates for subsets of the available data, with some subsets seemingly meeting the climate‐quality criteria. We find that seawater pH measurements on the total scale do not meet the climate‐quality criteria, though the inter‐consistency of these measurements improves (by 38%) when limited to the subset of measurements made using purified indicator dyes. We show that GLODAPv2 adjustments improve inter‐consistency for some subsets of the measurements while worsening it for others. Finally, we provide general guidance for quantifying the random uncertainty that applies for common combinations of measured and calculated values. 

Abstract. Climatologies, which depict mean fields of oceanographic variables on a regular geographic grid, and atlases, which provide graphical depictions of specific areas, play pivotal roles in comprehending the societal vulnerabilities linked to ocean acidification (OA). This significance is particularly pronounced in coastal regions where most economic activities, such as commercial and recreational fisheries and aquaculture industries, occur. In this paper, we unveil a comprehensive data product featuring coastal ocean acidification climatologies and atlases, encompassing the fugacity of carbon dioxide, pH on the total scale, total hydrogen ion content, free hydrogen ion content, carbonate ion content, aragonite saturation state, calcite saturation state, Revelle factor, total dissolved inorganic carbon content, and total alkalinity content. These variables are provided on 1° × 1° spatial grids at 14 standardized depth levels, ranging from the surface to a depth of 500 m, along the North American ocean margins, defined as the region between the coastline and a distance of 200 nautical miles (∼370 km) offshore. The climatologies and atlases were developed using the World Ocean Atlas (WOA) gridding methods of the NOAA National Centers for Environmental Information (NCEI) based on the recently released Coastal Ocean Data Analysis Product in North America (CODAP-NA), along with the 2021 update to the Global Ocean Data Analysis Project version 2 (GLODAPv2.2021) data product. The relevant variables were adjusted to the index year of 2010. The data product is available in NetCDF (https://doi.org/10.25921/g8pb-zy76, Jiang et al., 2022b) on the NOAA Ocean Carbon and Acidification Data System: https://www.ncei.noaa.gov/data/oceans/ncei/ocads/metadata/0270962.html (last access: 15 July 2024). It is recommended to use the objectively analyzed mean fields (with “_an” suffix) for each variable. The atlases can be accessed at https://www.ncei.noaa.gov/access/ocean-carbon-acidification-data-system/synthesis/nacoastal.html (last access: 15 July 2024). 

Abstract The temperature range of Earth's open‐ocean waters is roughly 0–30°C, yet our understanding of the seawater carbon dioxide (CO₂) system is largely derived from analyses conducted within a narrow temperature range (e.g., laboratory temperature of 20°C or 25°C). Herein, we address two aspects of open‐ocean CO₂‐system measurements and modeling: (1) a highly precise spectrophotometric technique is used to determine bicarbonate dissociation constants (K₂) in seawater at temperatures as low as 3°C and (2) a cruise dataset uniquely including total scale pH measurements at two temperatures is used for CO₂‐system internal consistency comparisons at 12°C and 25°C. Our pK₂parameterization (where pK = −logK) is applicable for broad ranges of salinity (20 ≤ S_P ≤ 40) and temperature (3°C ≤ t ≤ 35°C). Our CO₂‐system internal consistency evaluation (comparison of measured and calculated CO₂‐system parameters) utilized data obtained during NOAA's 2021 West Coast Ocean Acidification Cruise: total alkalinity (TA), total dissolved inorganic carbon (DIC), pH measured at 25°C, and pH measured at 12°C (n = 265). Results demonstrate that, relative to calculations utilizing the TA, DIC pair, agreement between measured and calculated parameters is improved when either TA or DIC is paired with pH measurements at either temperature. Calculations of CO₂fugacity (fCO₂) and aragonite saturation state (Ω_ar) using pH measurements made at 25°C or 12°C (paired with either TA or DIC) are statistically indistinguishable. Results also suggest that the temperature dependence of current CO₂‐system dissociation constants need further refinement. 

Abstract The ocean carbonate system is critical to monitor because it plays a major role in regulating Earth's climate and marine ecosystems. It is monitored using a variety of measurements, and it is commonly understood that all components of seawater carbonate chemistry can be calculated when at least two carbonate system variables are measured. However, several recent studies have highlighted systematic discrepancies between calculated and directly measured carbonate chemistry variables and these discrepancies have large implications for efforts to measure and quantify the changing ocean carbon cycle. Given this, the Ocean Carbonate System Intercomparison Forum (OCSIF) was formed as a working group through the Ocean Carbon and Biogeochemistry program to coordinate and recommend research to quantify and/or reduce uncertainties and disagreements in measurable seawater carbonate system measurements and calculations, identify unknown or overlooked sources of these uncertainties, and provide recommendations for making progress on community efforts despite these uncertainties. With this paper we aim to (1) summarize recent progress toward quantifying and reducing carbonate system uncertainties; (2) advocate for research to further reduce and better quantify carbonate system measurement uncertainties; (3) present a small amount of new data, metadata, and analysis related to uncertainties in carbonate system measurements; and (4) restate and explain the rationales behind several OCSIF recommendations. We focus on open ocean carbonate chemistry, and caution that the considerations we discuss become further complicated in coastal, estuarine, and sedimentary environments. 

Abstract. The Global Ocean Data Analysis Project (GLODAP) is a synthesis effort providing regular compilations of surface to bottom ocean biogeochemical bottle data, with an emphasis on seawater inorganic carbon chemistry and related variables determined through chemical analysis of seawater samples. GLODAPv2.2023 is an update of the previous version, GLODAPv2.2022 (Lauvset et al., 2022). The major changes are as follows: data from 23 new cruises were added. In addition, a number of changes were made to the data included in GLODAPv2.2022. GLODAPv2.2023 includes measurements from more than 1.4 million water samples from the global oceans collected on 1108 cruises. The data for the now 13 GLODAP core variables (salinity, oxygen, nitrate, silicate, phosphate, dissolved inorganic carbon, total alkalinity, pH, chlorofluorocarbon-11 (CFC-11), CFC-12, CFC-113, CCl4, and SF6) have undergone extensive quality control with a focus on the systematic evaluation of bias. The data are available in two formats: (i) as submitted by the data originator but converted to World Ocean Circulation Experiment (WOCE) exchange format and (ii) as a merged data product with adjustments applied to minimize bias. For the present annual update, adjustments for the 23 new cruises were derived by comparing those data with the data from the 1085 quality-controlled cruises in the GLODAPv2.2022 data product using crossover analysis. SF6 data from all cruises were evaluated by comparison with CFC-12 data measured on the same cruises. For nutrients and ocean carbon dioxide (CO2), chemistry comparisons to estimates based on empirical algorithms provided additional context for adjustment decisions. The adjustments that we applied are intended to remove potential biases from errors related to measurement, calibration, and data-handling practices without removing known or likely time trends or variations in the variables evaluated. The compiled and adjusted data product is believed to be consistent to better than 0.005 in salinity, 1 % in oxygen, 2 % in nitrate, 2 % in silicate, 2 % in phosphate, 4 µmol kg−1 in dissolved inorganic carbon, 4 µmol kg−1 in total alkalinity, 0.01–0.02 in pH (depending on region), and 5 % in the halogenated transient tracers. The other variables included in the compilation, such as isotopic tracers and discrete CO2 fugacity (fCO2), were not subjected to bias comparison or adjustments. The original data, their documentation, and DOI codes are available at the Ocean Carbon and Acidification Data System of NOAA National Centers for Environmental Information (NCEI), which also provides access to the merged data product. This is provided as a single global file and as four regional ones – the Arctic, Atlantic, Indian, and Pacific oceans – under https://doi.org/10.25921/zyrq-ht66 (Lauvset et al., 2023). These bias-adjusted product files also include significant ancillary and approximated data, which were obtained by interpolation of, or calculation from, measured data. This living data update documents the GLODAPv2.2023 methods and provides a broad overview of the secondary quality control procedures and results.