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The years since 2000 have been a golden age in in situ ocean observing with the proliferation and organization of autonomous platforms such as surface drogued buoys and subsurface Argo profiling floats augmenting ship-based observations. Global time series of mean sea surface temperature and ocean heat content are routinely calculated based on data from these platforms, enhancing our understanding of the ocean’s role in Earth’s climate system. Individual measurements of meteorological, sea surface, and subsurface variables directly improve our understanding of the Earth system, weather forecasting, and climate projections. They also provide the data necessary for validating and calibrating satellite observations. Maintaining this ocean observing system has been a technological, logistical, and funding challenge. The global COVID-19 pandemic, which took hold in 2020, added strain to the maintenance of the observing system. A survey of the contributing components of the observing system illustrates the impacts of the pandemic from January 2020 through December 2021. The pandemic did not reduce the short-term geographic coverage (days to months) capabilities mainly due to the continuation of autonomous platform observations. In contrast, the pandemic caused critical loss to longer-term (years to decades) observations, greatly impairing the monitoring of such crucial variables as ocean carbon and the state of the deep ocean. So, while the observing system has held under the stress of the pandemic, work must be done to restore the interrupted replenishment of the autonomous components and plan for more resilient methods to support components of the system that rely on cruise-based measurements.

The oceanic sink for anthropogenic CO2 (Cant) that humans have emitted into the atmosphere has been pivotal for limiting global warming. The transport of Cant from the surface into the ocean interior, where most of it is accumulating, is the rate limiting step for this uptake. Yet multi-decadal trends in the ocean interior storage of Cant have not been assessed at global scale. We determined such trends by applying the eMLR(C*) regression method to ocean interior observations collected between 1989 and 2020, and found that the global ocean storage of Cant grew by 29 ± 3 Pg C dec-1 and 27 ± 3 Pg C dec-1 (±1σ) from 1994 to 2004 and 2004 to 2014, respectively. Although the two growth rates are not significantly different, they imply a reduction of the oceanic uptake fraction of the anthropogenic emissions from 36 ± 4 % to 27 ± 3 % during the respective decades. We attribute this reduction to a decrease of the ocean buffer capacity and changes in ocean circulation. In the Atlantic Ocean, the maximum storage rate shifted from the Northern to the Southern Hemisphere, plausibly caused by a weaker formation rate of North Atlantic Deep Waters and an intensified ventilation of mode and intermediate waters in the Southern Hemisphere. Between 1994 and 2004, the oceanic Cant accumulation exceeded the net air-sea flux by 8 ± 4 Pg C dec-1, suggesting a loss of natural carbon from the ocean during this decade. Our results reveal a substantial vulnerability of the ocean carbon sink.

25 pages, 10 figures, 7 tables.-- This work is distributed under the Creative Commons Attribution 4.0 License, 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. GLODAPv2.2021 is an update of the previous version, GLODAPv2.2020 (Olsen et al., 2020). The major changes are as follows: data from 43 new cruises were added, data coverage was extended until 2020, all data with missing temperatures were removed, and a digital object identifier (DOI) was included for each cruise in the product files. In addition, a number of minor corrections to GLODAPv2.2020 data were performed. GLODAPv2.2021 includes measurements from more than 1.3 million water samples from the global oceans collected on 989 cruises. The data for the 12 GLODAP core variables (salinity, oxygen, nitrate, silicate, phosphate, dissolved inorganic carbon, total alkalinity, pH, CFC-11, CFC-12, CFC-113, and CCl4) have undergone extensive quality control with a focus on systematic evaluation of bias. The data are available in two formats: (i) as submitted by the data originator but updated to World Ocean Circulation Experiment (WOCE) exchange format and (ii) as a merged data product with adjustments applied to minimize bias. For this annual update, adjustments for the 43 new cruises were derived by comparing those data with the data from the 946 quality controlled cruises in the GLODAPv2.2020 data product using crossover analysis. Comparisons to estimates of nutrients and ocean CO2 chemistry based on empirical algorithms provided additional context for adjustment decisions in this version. The adjustments 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 with to better than 0.005 in salinity, 1% in oxygen, 2% in nitrate, 2% in silicate, 2% in phosphate, 4 μmolkg-1 in dissolved inorganic carbon, 4 μmolkg-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 Data System of NOAA NCEI (https://www.ncei.noaa.gov/access/ocean-carbon-data-system/oceans/GLODAPv2_2021/, last access: 7 July 2021). This site also provides access to the merged data product, which 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/ttgq-n825 (Lauvset et al., 2021). These bias-adjusted product files also include significant ancillary and approximated data and can be accessed via https://www.glodap.info (last access: 29 June 2021). These were obtained by interpolation of, or calculation from, measured data. This living data update documents the GLODAPv2.2021 methods and provides a broad overview of the secondary quality control procedures and results, This research has been supported by EU Horizon 2020 through the EuroSea action (grant no. 862626), internal strategic funding from NORCE Climate, Prociencia/UERJ (grant 2019–2021), IEO RADIALES and RADPROF projects, the UK Climate Linked Atlantic Sector Science (CLASS) NERC National Capability Long-term Single Centre Science Programme(grant no. NE/R015953/1), the BOCATS2 (PID2019-104279GBC21) project funded by MCIN/AEI/10.13039/501100011033 and contributing toWATER:iOS CSIC PTI, the NOAA Global Observations and Monitoring Division (fund reference 100007298), the Office of Oceanic and Atmospheric Research of NOAA Global Observations and Monitoring Division (fund reference 100007298), the Office of Oceanic and Atmospheric Research of NOAA, the BONUS INTEGRAL project (grant no. 03F0773A), the Australian Antarctic Program Partnership and the Integrated Marine Observing System, EU Horizon 2020 action SO-CHIC (grant no. 821001), and the Initiative and Networking Fund of the Helmholtz Association through the project “Digital Earth” (grant no. ZT-0025)

We introduce three new Empirical Seawater Property Estimation Routines (ESPERs) capable of predicting seawater phosphate, nitrate, silicate, oxygen, total titration seawater alkalinity, total hydrogen scale pH (pHT), and total dissolved inorganic carbon (DIC) from up to 16 combinations of seawater property measurements. The routines generate estimates from neural networks (ESPER_NN), locally interpolated regressions (ESPER_LIR), or both (ESPER_Mixed). They require a salinity value and coordinate information, and benefit from additional seawater measurements if available. These routines are intended for seawater property measurement quality control and quality assessment, generating estimates for calculations that require approximate values, original science, and producing biogeochemical property context from a data set. Relative to earlier LIR routines, the updates expand their functionality, including new estimated properties and combinations of predictors, a larger training data product including new cruises from the 2020 Global Data Analysis Project data product release, and the implementation of a first-principles approach for quantifying the impacts of anthropogenic carbon on DIC and pHT. We show that the new routines perform at least as well as existing routines, and, in some cases, outperform existing approaches, even when limited to the same training data. Given that additional training data has been incorporated into these updated routines, these updates should be considered an improvement over earlier versions. The routines are intended for all ocean depths for the interval from 1980 to ~2030 c.e., and we caution against using the routines to directly quantify surface ocean seasonality or make more distant predictions of DIC or pHT., 1,823

Accurate assessment of anthropogenic carbon dioxide (CO2) emissions and their redistribution among the atmosphere, ocean, and terrestrial biosphere in a changing climate is critical to better understand the global carbon cycle, support the development of climate policies, and project future climate change. Here we describe and synthesise data sets and methodology to quantify the five major components of the global carbon budget and their uncertainties. Fossil CO2 emissions (EFOS) are based on energy statistics and cement production data, while emissions from land-use change (ELUC), mainly deforestation, are based on land-use and land-use change data and bookkeeping models. Atmospheric CO2 concentration is measured directly, and its growth rate (GATM) is computed from the annual changes in concentration. The ocean CO2 sink (SOCEAN) is estimated with global ocean biogeochemistry models and observation-based data-products. The terrestrial CO2 sink (SLAND) is estimated with dynamic global vegetation models. The resulting carbon budget imbalance (BIM), the difference between the estimated total emissions and the estimated changes in the atmosphere, ocean, and terrestrial biosphere, is a measure of imperfect data and understanding of the contemporary carbon cycle. All uncertainties are reported as ±1σ. For the year 2021, EFOS increased by 5.1 % relative to 2020, with fossil emissions at 10.1 ± 0.5 GtC yr-1 (9.9 ± 0.5 GtC yr-1 when the cement carbonation sink is included), ELUC was 1.1 ± 0.7 GtC yr-1, for a total anthropogenic CO2 emission of 11.1 ± 0.8 GtC yr-1 (40.8 ± 2.9 GtCO2). Also, for 2021, GATM was 5.2 ± 0.2 GtC yr-1 (2.5 ± 0.1 ppm yr-1), SOCEAN was 2.9 ± 0.4 GtC yr-1 and SLAND was 3.5 ± 0.9 GtC yr-1, with a BIM of -0.6 GtC yr-1 (i.e. total estimated sources too low or sinks too high). The global atmospheric CO2 concentration averaged over 2021 reached 414.71 ± 0.1 ppm. Preliminary data for 2022, suggest an increase in EFOS relative to 2021 of +1.1 % (0 % to 1.7 %) globally, and atmospheric CO2 concentration reaching 417.3 ppm, more than 50 % above pre-industrial level. Overall, the mean and trend in the components of the global carbon budget are consistently estimated over the period 1959–2021, but discrepancies of up to 1 GtC yr-1 persist for the representation of annual to semi-decadal variability in CO2 fluxes. Comparison of estimates from multiple approaches and observations shows: (1) a persistent large uncertainty in the estimate of land-use changes emissions, (2) a low agreement between the different methods on the magnitude of the land CO2 flux in the northern extra-tropics, and (3) a discrepancy between the different methods on the strength of the ocean sink over the last decade. This living data update documents changes in the methods and data sets used in this new global carbon budget and the progress in understanding of the global carbon cycle compared with previous publications of this data set (Friedlingstein et al., 2022a; Friedlingstein et al., 2020; Friedlingstein et al., 2019; Le Quéré et al., 2018b, 2018a, 2016, 2015b, 2015a, 2014, 2013). The data presented in this work are available at https://doi.org/10.18160/GCP-2022 (Friedlingstein et al., 2022b).

The ocean absorbs approximately a quarter of the carbon dioxide currently released to the atmosphere by human activities (Canth). A disproportionately large fraction accumulates in the North Atlantic due to the combined effects of transport by the Atlantic Meridional Overturning Circulation (AMOC) and air–sea exchange. However, discrepancies exist between modelled and observed estimates of the air–sea exchange due to unresolved ocean transport variability. Here we quantify the strength and variability of Canth transports across 26.5° N in the North Atlantic between 2004 and 2012 using circulation measurements from the RAPID mooring array and hydrographic observations. Over this period, decreasing circulation strength tended to decrease northward Canth transport, while increasing Canth concentrations (preferentially in the upper limb of the overturning circulation) tended to increase northward Canth transport. These two processes compensated each other over the 8.5-year period. While ocean transport and air–sea Canth fluxes are approximately equal in magnitude, the increasing accumulation rate of Canth in the North Atlantic combined with a stable ocean transport supply means we infer a growing contribution from air–sea Canth fluxes over the period. North Atlantic Canth accumulation is thus sensitive to AMOC strength, but growing atmospheric Canth uptake continues to significantly impact Canth transports. Slowdown of the Atlantic Meridional Overturning Circulation from 2004 to 2012 led to a decrease in its relative contribution to North Atlantic carbon accumulation, while the supply from air–sea fluxes increased, according to an analysis of ocean mooring circulation observations.

Internally consistent, quality-controlled (QC) data products play an important role in promoting regional-to-global research efforts to understand societal vulnerabilities to ocean acidification (OA). However, there are currently no such data products for the coastal ocean, where most of the OA-susceptible commercial and recreational fisheries and aquaculture industries are located. In this collaborative effort, we compiled, quality-controlled, and synthesized 2 decades of discrete measurements of inorganic carbon system parameters, oxygen, and nutrient chemistry data from the North American continental shelves to generate a data product called the Coastal Ocean Data Analysis Product in North America (CODAP-NA). There are few deep-water (> 1500 m) sampling locations in the current data product. As a result, crossover analyses, which rely on comparisons between measurements on different cruises in the stable deep ocean, could not form the basis for cruise-to-cruise adjustments. For this reason, care was taken in the selection of data sets to include in this initial release of CODAP-NA, and only data sets from laboratories with known quality assurance practices were included. New consistency checks and outlier detections were used to QC the data. Future releases of this CODAP-NA product will use this core data product as the basis for cruise-to-cruise comparisons. We worked closely with the investigators who collected and measured these data during the QC process. This version (v2021) of the CODAP-NA is comprised of 3391 oceanographic profiles from 61 research cruises covering all continental shelves of North America, from Alaska to Mexico in the west and from Canada to the Caribbean in the east. Data for 14 variables (temperature; salinity; dissolved oxygen content; dissolved inorganic carbon content; total alkalinity; pH on total scale; carbonate ion content; fugacity of carbon dioxide; and substance contents of silicate, phosphate, nitrate, nitrite, nitrate plus nitrite, and ammonium) have been subjected to extensive QC. CODAP-NA is available as a merged data product (Excel, CSV, MATLAB, and NetCDF; https://doi.org/10.25921/531n-c230, https://www.ncei.noaa.gov/data/oceans/ncei/ocads/metadata/0219960.html, last access: 15 May 2021) (Jiang et al., 2021a). The original cruise data have also been updated with data providers' consent and summarized in a table with links to NOAA's National Centers for Environmental Information (NCEI) archives (https://www.ncei.noaa.gov/access/ocean-acidification-data-stewardship-oads/synthesis/NAcruises.html).

State of the climate in 2019

A high-quality dataset of surface water fugacity of CO2 (fCO2w)1, consisting of over a million observations, and derived products are presented for the northern Caribbean Sea, covering the time span from 2002 through 2018. Prior to installation of automated pCO2 systems on cruise ships of Royal Caribbean International and subsidiaries, very limited surface water carbon data were available in this region. With this observational program, the northern Caribbean Sea has now become one of the best-sampled regions for pCO2 of the world ocean. The dataset and derived quantities are binned and averaged on a 1∘ monthly grid and are available at http://accession.nodc.noaa.gov/0207749 (last access: 30 June 2020) (https://doi.org/10.25921/2swk-9w56; Wanninkhof et al., 2019a). The derived quantities include total alkalinity (TA), acidity (pH), aragonite saturation state (ΩAr) and air–sea CO2 flux and cover the region from 15 to 28∘ N and 88 to 62∘ W. The gridded data and products are used for determination of status and trends of ocean acidification, for quantifying air–sea CO2 fluxes and for ground-truthing models. Methodologies to derive the TA, pH and ΩAr and to calculate the fluxes from fCO2w temperature and salinity are described.

Ocean acidification (OA) progression is affected by multiple factors, such as ocean warming, biological production, and runoff. Here we used an ocean-biogeochemical model to assess the impact of ri...

The North Brazil Current (NBC) flows northward across the Equator, passes the mouth of the Amazon River, and forms large oceanic eddies near 8° N. We investigate the processes driving the variability of air-sea CO2 fluxes at different scales in early 2020 in the region [50° W–59° W–5° N–16° N]. This region is a pathway between the equatorial and North Atlantic Ocean and was surveyed during the EUREC4A-OA/ATOMIC campaign. In-situ surface fugacity of CO2 (fCO2), salinity and temperature combined with maps of satellite salinity, chlorophyll-a and temperature highlight contrasting properties in the region. In February 2020, the area is a CO2 sink (−1.7 TgC.month−1), previously underestimated by a factor 10. The NBC rings transport saline and high fCO2 water indicative of their equatorial origins and are a small source of CO2 at regional scale. Their main impact on the variability of biogeochemical parameters is through the filaments they entrain into the open ocean. During the campaign, a nutrient-rich freshwater plume from the Amazon River is entrained from the shelf up to 12° N and caused a phytoplankton bloom leading to a significant carbon drawdown (~20 % of the total sink). On the other hand, saltier filaments of shelf water rich in detrital material act as strong local sources of CO2. Spatial distribution of fCO2 is therefore strongly influenced by ocean dynamics south of 12° N. The less variable North Atlantic subtropical water extends from Barbados northward. They represent ~60 % of the total sink due to their lower temperature associated with winter cooling and strong winds.

4 pages, 1 figure.-- This article is licensed under a Creative Commons Attribution 4.0 International License, The ocean is mitigating global warming by absorbing large amounts of excess carbon dioxide from human activities. To quantify and monitor the ocean carbon sink, we need a state-of-the-art data resource that makes data submission and retrieval machine-compatible and efficient, This effort has been supported by EU Horizon 2020 through the EuroSea action (grant no. 862626), the Helmholtz Association through “Digital Earth” (grant no. ZT-0025), L.C.C. acknowledges the UERJ/Prociencia grant (2018-2021), M.H. acknowledge EU Horizon 2020 action SO-CHIC (grant N°821001). B.C., R.A.F., E.B., K.O’.B., and R.W. were supported by NOAA/OAR and NOAA/GOMO (fund ref. 100007298), B.T. was partly supported by Australia’s Integrated Marine Observing System (IMOS), S.K.L. acknowledges internal strategic funding from NORCE Climate, M.T. acknowledges support from the US NSF grant OCE-1840868 to SCOR. The PMEL and CICOES contributions are 5253 and 2020-1141, respectively

Surface seawater partial pressure of CO2 (pCO2) is a critical parameter in the quantification of air-sea CO2 flux, which further plays an important role in quantifying the global carbon budget and understanding ocean acidification. Yet, the remote estimation of pCO2 in coastal waters (under influences of multiple processes) has been difficult due to complex relationships between environmental variables and surface pCO2. To date there is no unified model to remotely estimate surface pCO2 in oceanic regions that are dominated by different oceanic processes. In our study area, the Gulf of Mexico (GOM), this challenge is addressed through the evaluation of different approaches, including multi-linear regression (MLR), multi-nonlinear regression (MNR), principle component regression (PCR), decision tree, supporting vector machines (SVMs), multilayer perceptron neural network (MPNN), and random forest based regression ensemble (RFRE). After modeling, validation, and extensive tests using independent cruise datasets, the RFRE model proved to be the best approach. The RFRE model was trained using data comprised of extensive pCO2 datasets (collected over 16 years by many groups) and MODIS (Moderate Resolution Imaging Spectroradiometer) estimated sea surface temperature (SST), sea surface salinity (SSS), surface chlorophyll concentration (Chl), and diffuse attenuation of downwelling irradiance (Kd). This RFRE-based pCO2 model allows for the estimation of surface pCO2 from satellites with a spatial resolution of ~1 km. It showed an overall performance of a root mean square difference (RMSD) of 9.1 μatm, with a coefficient of determination (R2) of 0.95, a mean bias (MB) of −0.03 μatm, a mean ratio (MR) of 1.00, an unbiased percentage difference (UPD) of 0.07%, and a mean ratio difference (MRD) of 0.12% for pCO2 ranging between 145 and 550 μatm. The model, with its original parameterization, has been tested with independent datasets collected over the entire GOM, with satisfactory performance in each case (RMSD of ≤~10 μatm for open GOM waters and RMSD of ≤~25 μatm for coastal and river-dominated waters). The sensitivity of the RFRE-based pCO2 model to uncertainties of each input environmental variable was also thoroughly examined. The results showed that all induced uncertainties were close to, or within, the uncertainty of the model itself with higher sensitivity to uncertainties in SST and SSS than to uncertainties in Chl and Kd. The extensive validation, evaluation, and sensitivity analysis indicate the robustness of the RFRE model in estimating surface pCO2 for the range of 145–550 μatm in most GOM waters. The RFRE model approach was applied to the Gulf of Maine (a contrasting oceanic region to GOM), with local model training. The results showed significant improvement over other models suggesting that the RFRE may serve as a robust approach for other regions once sufficient field-measured pCO2 data are available for model training.

8 pages, 2 tables, 4 figures, We quantify the oceanic sink for anthropogenic carbon dioxide (CO2) over the period 1994 to 2007 by using observations from the global repeat hydrography program and contrasting them to observations from the 1990s. Using a linear regression–based method, we find a global increase in the anthropogenic CO2 inventory of 34 ± 4 petagrams of carbon (Pg C) between 1994 and 2007. This is equivalent to an average uptake rate of 2.6 ± 0.3 Pg C year−1 and represents 31 ± 4% of the global anthropogenic CO2 emissions over this period. Although this global ocean sink estimate is consistent with the expectation of the ocean uptake having increased in proportion to the rise in atmospheric CO2, substantial regional differences in storage rate are found, likely owing to climate variability–driven changes in ocean circulation, We are grateful to the many funding agencies in the various countries that financially supported the global ship-based surveys that underpin much of this work. In particular, we acknowledge funding from the U.S. National Science Foundation and from the National Oceanic and Atmospheric Administration (NOAA), and the GO-SHIP program together with the International ocean carbon coordination project (IOCCP), for their efforts to initiate and coordinate the repeat hydrography program. The work of N.G. and D.C. was supported by ETH and the FP7 projects CarboChange (264879) and Geocarbon (283080). S.v.H. also received support from CarboChange (264879). R.W., R.A.F., and B.R.C. acknowledge the support of Oceanic and Atmospheric Research NOAA and the U.S. Department of Commerce, including resources from the NOAA Global Ocean Monitoring and Observations Division (fund reference 100007298). This is contribution no. 4796 from the NOAA Pacific Marine Environmental Laboratory and JISAO contribution 2018-0185. M.I. acknowledges support from the Japan Meteorological Agency and MEXT KAKENHI grant no. 24121003 “NEOPS” and JP16H01594 “OMIX”. S.K.L. acknowledges support from the Research Council of Norway (214513). F.F.P. was supported by Ministerio de Economía y Competitividad through the ARIOS (CTM2016-76146-C3-1-R) project cofunded by the Fondo Europeo de Desarrollo Regional 2014-2020 (FEDER) and EU Horizon 2020 through the AtlantOS project (grant agreement 633211)

By means of a variety of international observing and modeling efforts, the ocean carbon community has developed numerous estimates for ocean carbon uptake. In this presentation, we report on the synthesis effort we are undertaking under the auspices of an Ocean Carbon and Biogeochemistry Working Group. Our initial goal for this working group is to determine the best estimate for the net and anthropogenic carbon sink from 1994-2007 based on three approaches that independently use interior data, surface data or hindcast ocean models. Combining two approaches that use interior ocean data to estimate anthropogenic carbon, Fant = -2.40+-0.21 PgC/yr (2 sigma uncertainty). Estimates for the net, or contemporary, ocean carbon uptake come from 6 products that interpolate surface ocean pCO2 data to global coverage: Fnet = -1.58+-0.19 PgC/yr for 1994-2007. Uncertain closure terms for naturally-outgassed river-derived carbon and non-steady state natural carbon fluxes in the open ocean are then added to derive Fant from surface observation-based Fnet. Ocean models do not include river-derived carbon, but do include non-steady state natural carbon fluxes, and thus a third estimate for Fant is derived. The combined best-estimate is Fant = -2.35+-0.53 PgC/yr. We detail the uncertainties and assumptions made in deriving these estimates, and suggest paths forward to further reduce uncertainties.

Strong winds in Southern Ocean storms drive air-sea carbon and heat fluxes. These fluxes are integral to the global climate system and the wind speeds that drive them are increasing. The current sc...

Internally-consistent, quality-controlled data products play a very important role in promoting regional to global research efforts to understand societal vulnerabilities to ocean acidification (OA). However, there are currently no such data products for the coastal ocean where most of the OA-susceptible commercial and recreational fisheries and aquaculture industries are located. In this collaborative effort, we compiled, quality controlled (QC), and synthesized two decades of discrete measurements of inorganic carbon system parameters, oxygen, and nutrient chemistry data from the U.S. North American continental shelves, to generate a data product called the Coastal Ocean Data Analysis Product for North America (CODAP-NA). There are few deep-water (> 1500 m) sampling locations in the current data product. As a result, cross-over analyses, which rely on comparisons between measurements on different cruises in the stable deep ocean, could not form the basis for cruise-to-cruise adjustments. For this reason, care was taken in the selection of data sets to include in this initial release of CODAP-NA, and only data sets from laboratories with known quality assurance practices were included. New consistency checks and outlier detections were used to QC the data. Future releases of this CODAP-NA product will use this core data product as the basis for secondary QC. We worked closely with the investigators who collected and measured these data during the QC process. This version of the CODAP-NA is comprised of 3,292 oceanographic profiles from 61 research cruises covering all continental shelves of North America, from Alaska to Mexico in the west and from Canada to the Caribbean in the east. Data for 14 variables (temperature; salinity; dissolved oxygen concentration; dissolved inorganic carbon concentration; total alkalinity; pH on the Total Scale; carbonate ion concentration; fugacity of carbon dioxide; and concentrations of silicate, phosphate, nitrate, nitrite, nitrate plus nitrite, and ammonium) have been subjected to extensive QC. CODAP-NA is available as a merged data product (Excel, CSV, MATLAB, and NetCDF, https://doi.org/10.25921/531n-c230, https://www.ncei.noaa.gov/data/oceans/ncei/ocads/metadata/0219960.html) (Jiang et al., 2020). The original cruise data have also been updated with data providers' consent and summarized in a table with links to NOAA's National Centers for Environmental Information (NCEI) archives (https://www.ncei.noaa.gov/access/ocean-acidification-data-stewardship-oads/synthesis/NAcruises.html).

EGU General Assembly 2021, online, 19–30 April 2021.-- This work is distributed under the Creative Commons Attribution 4.0 License, Surface ocean pCO2-based estimates and models indicate that the ocean sink for anthropogenic CO2 (Cant) has continued to increase unabatedly over the past decade. However, the most recent global and observation-based estimate of the accumulation of Cant in the ocean interior by Gruber et al. (2019) does not extend beyond 2007, preventing an independent assessment of this increase in the magnitude of the sink

26 pages, 11 figures, 7 tables.-- This work is distributed under the Creative Commons Attribution 4.0 License, The Global Ocean Data Analysis Project (GLODAP) is a synthesis effort providing regular compilations of surface-to-bottom ocean biogeochemical data, with an emphasis on seawater inorganic carbon chemistry and related variables determined through chemical analysis of seawater samples. GLODAPv2.2020 is an update of the previous version, GLODAPv2.2019. The major changes are data from 106 new cruises added, extension of time coverage to 2019, and the inclusion of available (also for historical cruises) discrete fugacity of CO2 (fCO2) values in the merged product files. GLODAPv2.2020 now includes measurements from more than 1.2 million water samples from the global oceans collected on 946 cruises. The data for the 12 GLODAP core variables (salinity, oxygen, nitrate, silicate, phosphate, dissolved inorganic carbon, total alkalinity, pH, CFC-11, CFC-12, CFC-113, and CCl4) have undergone extensive quality control with a focus on systematic evaluation of bias. The data are available in two formats: (i) as submitted by the data originator but updated to WOCE exchange format and (ii) as a merged data product with adjustments applied to minimize bias. These adjustments were derived by comparing the data from the 106 new cruises with the data from the 840 quality-controlled cruises of the GLODAPv2.2019 data product using crossover analysis. Comparisons to empirical algorithm estimates provided additional context for adjustment decisions; this is new to this version. The adjustments 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 μmolkg-1 in dissolved inorganic carbon, 4 μmolkg-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 fCO2, were not subjected to bias comparison or adjustments. The original data and their documentation and DOI codes are available at the Ocean Carbon Data System of NOAA NCEI (https://www.nodc.noaa.gov/ocads/oceans/GLODAPv2_2020/, last access: 20 June 2020). This site also provides access to the merged data product, which is provided as a single global file and as four regional ones – the Arctic, Atlantic, Indian, and Pacific oceans – under https://doi.org/10.25921/2c8h-sa89 (Olsen et al., 2020). These bias-adjusted product files also include significant ancillary and approximated data. These were obtained by interpolation of, or calculation from, measured data. This living data update documents the GLODAPv2.2020 methods and provides a broad overview of the secondary quality control procedures and results, Nico Lange was funded by EU Horizon 2020 through the EuroSea action (grant no. 862626). Leticia Cotrim da Cunha was supported by Prociencia/UERJ (grant no. 2019-2021). Marta Álvarez was supported by the IEO RADIALES and RADPROF projects. Peter J. Brown was partially funded by the UK Climate Linked Atlantic Sector Science (CLASS) NERC National Capability Long-term Single Centre Science Programme (grant no. NE/R015953/1). Anton Velo and Fiz F. Pérez were supported by the BOCATS2 Project (grant no. PID2019-104279GBC21) co-funded by the Spanish Government and the Fondo Europeo de Desarrollo Regional (FEDER). RikWanninkhof and Brendan R. Carter were supported by the NOAA Global Observations and Monitoring Division (fund reference 100007298) and the Office of Oceanic and Atmospheric Research of NOAA. Henry C. Bittig has been supported by the BONUS INTEGRAL project (grant no. 03F0773A). This research was also funded by the Initiative and Networking Fund of the Helmholtz Association through the project “Digital Earth” (grant no. ZT-0025)

The Global Ocean Data Analysis Project (GLODAP) is a synthesis effort providing regular compilations of surface to bottom ocean biogeochemical data, with an emphasis on seawater inorganic carbon chemistry and related variables determined through chemical analysis of water samples. GLODAPv2.2020 is an update of the previous version, GLODAPv2.2019. The major changes are: data from 106 more cruises added, extension of time coverage until 2019, and the inclusion of available discrete fugacity of CO2 (fCO2) values in the merged product files. GLODAPv2.2020 includes measurements from more than 1.2 million water samples from the global oceans collected on 946 cruises. The data for the 12 GLODAP core variables (salinity, oxygen, nitrate, silicate, phosphate, dissolved inorganic carbon, total alkalinity, pH, CFC-11, CFC-12, CFC-113, and CCl4) have undergone extensive quality control, especially systematic evaluation of bias. The data are available in two formats: (i) as submitted by the data originator but updated to WOCE exchange format and (ii) as a merged data product with adjustments applied to minimize bias. These adjustments were derived by comparing the data from the 106 new cruises with the data from the 840 quality-controlled cruises of the GLODAPv2.2019 data product. They correct for errors related to measurement, calibration, and data handling practices, while taking into account any 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, depending on region, in pH, and 5 % in the halogenated transient tracers. The other variables included in the compilation, such as isotopic tracers and discrete fCO2 were not subjected to bias comparison or adjustments. The original data, their documentation and doi codes are available at the Ocean Carbon Data System of NOAA NCEI (https://www.nodc.noaa.gov/ocads/oceans/GLODAPv2_2020/, last access: 22 June 2020). This site also provides access to the merged data product, which is provided as a single global file and as four regional ones – the Arctic, Atlantic, Indian, and Pacific oceans – under https://doi.org/10.25921/2c8h-sa89 (Olsen et al., 2020). The bias corrected product files also include significant ancillary and approximated data. These were obtained by interpolation of, or calculation from, measured data. This living data update documents the GLODAPv2.2020 methods and provides a broad overview of the secondary quality control procedures and results.

Uncertainties in carbon chemistry variability still remain large in the Gulf of Mexico (GoM), as data gaps limit our ability to infer basin-wide patterns. Here we configure and validate a regional high-resolution ocean biogeochemical model for the GoM to describe seasonal patterns in surface pressure of CO2 (pCO2), aragonite saturation state (ΩAr), and sea–air CO2 flux. Model results indicate that seasonal changes in surface pCO2 are strongly controlled by temperature across most of the GoM basin, except in the vicinity of the Mississippi–Atchafalaya river system delta, where runoff largely controls dissolved inorganic carbon (DIC) and total alkalinity (TA) changes. Our model results also show that seasonal patterns of surface ΩAr are driven by seasonal changes in DIC and TA, and reinforced by the seasonal changes in temperature. Simulated sea–air CO2 fluxes are consistent with previous observation-based estimates that show CO2 uptake during winter–spring, and CO2 outgassing during summer–fall. Annually, our model indicates a basin-wide mean CO2 uptake of 0.35 molm-2yr-1, and a northern GoM shelf (< 200 m) uptake of 0.93 molm-2yr-1. The observation and model-derived patterns of surface pCO2 and CO2 fluxes show good correspondence; thus this study contributes to improved constraints of the carbon budget in the region.

Syntheses of carbonate chemistry spatial patterns are important for predicting ocean acidification impacts, but are lacking in coastal oceans. Here, we show that along the North American Atlantic and Gulf coasts the meridional distributions of dissolved inorganic carbon (DIC) and carbonate mineral saturation state (Ω) are controlled by partial equilibrium with the atmosphere resulting in relatively low DIC and high Ω in warm southern waters and the opposite in cold northern waters. However, pH and the partial pressure of CO2 (pCO2) do not exhibit a simple spatial pattern and are controlled by local physical and net biological processes which impede equilibrium with the atmosphere. Along the Pacific coast, upwelling brings subsurface waters with low Ω and pH to the surface where net biological production works to raise their values. Different temperature sensitivities of carbonate properties and different timescales of influencing processes lead to contrasting property distributions within and among margins., Anthropogenic CO2 is acidifying the ocean, but knowledge of the carbonate properties underlying these dynamics in coastal oceans is lacking. Here, the authors reveal spatial distribution patterns and variability in carbonate chemistry along North America’s coasts.