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1. Surface Ocean CO2 Atlas Database Version 2022 (SOCATv2022) (NCEI Accession 0253659)

   https://doi.org/10.25921/1h9f-nb73  

   Bakker, Dorothee C. ; Alin, Simone R. ; Becker, Meike ; Bittig, Henry C. ; Castaño-Primo, Rocío ; Feely, Richard A. ; Gkritzalis, Thanos ; Kadono, Koji ; Kozyr, Alex ; Lauvset, Siv K. ; et al ( January 2022 , NOAA National Centers for Environmental Information)

   This dataset consists of the Surface Ocean CO2 Atlas Version 2022 (SOCATv2022) data product files. The ocean absorbs one quarter of the global CO2 emissions from human activity. The community-led Surface Ocean CO2 Atlas (www.socat.info) is key for the quantification of ocean CO2 uptake and its variation, now and in the future. SOCAT version 2022 has quality-controlled in situ surface ocean fCO2 (fugacity of CO2) measurements on ships, moorings, autonomous and drifting surface platforms for the global oceans and coastal seas from 1957 to 2021. The main synthesis and gridded products contain 33.7 million fCO2 values with an estimated accuracy of better than 5 μatm. A further 6.4 million fCO2 sensor data with an estimated accuracy of 5 to 10 μatm are separately available. During quality control, marine scientists assign a flag to each data set, as well as WOCE flags of 2 (good), 3 (questionable) or 4 (bad) to individual fCO2 values. Data sets are assigned flags of A and B for an estimated accuracy of better than 2 μatm, flags of C and D for an accuracy of better than 5 μatm and a flag of E for an accuracy of better than 10 μatm. Bakker et al. (2016) describe the quality control criteria used in SOCAT versions 3 to 2022. Quality control comments for individual data sets can be accessed via the SOCAT Data Set Viewer (www.socat.info). All data sets, where data quality has been deemed acceptable, have been made public. The main SOCAT synthesis files and the gridded products contain all data sets with an estimated accuracy of better than 5 µatm (data set flags of A to D) and fCO2 values with a WOCE flag of 2. Access to data sets with an estimated accuracy of 5 to 10 (flag of E) and fCO2 values with flags of 3 and 4 is via additional data products and the Data Set Viewer (Table 8 in Bakker et al., 2016). SOCAT publishes a global gridded product with a 1° longitude by 1° latitude resolution. A second product with a higher resolution of 0.25° longitude by 0.25° latitude is available for the coastal seas. The gridded products contain all data sets with an estimated accuracy of better than 5 µatm (data set flags of A to D) and fCO2 values with a WOCE flag of 2. Gridded products are available monthly, per year and per decade. Two powerful, interactive, online viewers, the Data Set Viewer and the Gridded Data Viewer (www.socat.info), enable investigation of the SOCAT synthesis and gridded data products. SOCAT data products can be downloaded. Matlab code is available for reading these files. Ocean Data View also provides access to the SOCAT data products (www.socat.info). SOCAT data products are discoverable, accessible and citable. The SOCAT Data Use Statement (www.socat.info) asks users to generously acknowledge the contribution of SOCAT scientists by invitation to co-authorship, especially for data providers in regional studies, and/or reference to relevant scientific articles. The SOCAT website (www.socat.info) provides a single access point for online viewers, downloadable data sets, the Data Use Statement, a list of contributors and an overview of scientific publications on and using SOCAT. Automation of data upload and initial data checks allows annual releases of SOCAT from version 4 onwards. SOCAT is used for quantification of ocean CO2 uptake and ocean acidification and for evaluation of climate models and sensor data. SOCAT products inform the annual Global Carbon Budget since 2013. The annual SOCAT releases by the SOCAT scientific community are a Voluntary Commitment for United Nations Sustainable Development Goal 14.3 (Reduce Ocean Acidification) (#OceanAction20464). More broadly the SOCAT releases contribute to UN SDG 13 (Climate Action) and SDG 14 (Life Below Water), and to the UN Decade of Ocean Science for Sustainable Development. Hundreds of peer-reviewed scientific publications and high-impact reports cite SOCAT. The SOCAT community-led synthesis product is a key step in the value chain based on in situ inorganic carbon measurements of the oceans, which provides policy makers with critical information on ocean CO2 uptake in climate negotiations. The need for accurate knowledge of global ocean CO2 uptake and its (future) variation makes sustained funding of in situ surface ocean CO2 observations imperative. 

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2. A uniform <i>p</i>CO₂ climatology combining open and coastal oceans

   https://doi.org/10.5194/essd-12-2537-2020  

   Landschützer, Peter ; Laruelle, Goulven G. ; Roobaert, Alizee ; Regnier, Pierre ( January 2020 , Earth System Science Data)

   null (Ed.)

   Abstract. In this study, we present the first combined open- and coastal-ocean pCO2 mapped monthly climatology (Landschützer et al., 2020b, https://doi.org/10.25921/qb25-f418, https://www.nodc.noaa.gov/ocads/oceans/MPI-ULB-SOM_FFN_clim.html, last access: 8 April 2020) constructed from observations collected between 1998 and 2015 extracted from the Surface Ocean CO2 Atlas (SOCAT) database. We combine two neural network-based pCO2 products, one from the open ocean and the other from the coastal ocean, and investigate their consistency along their common overlap areas. While the difference between open- and coastal-ocean estimates along the overlap area increases with latitude, it remains close to 0 µatm globally. Stronger discrepancies, however, exist on the regional level resulting in differences that exceed 10 % of the climatological mean pCO2, or an order of magnitude larger than the uncertainty from state-of-the-art measurements. This also illustrates the potential of such an analysis to highlight where we lack a good representation of the aquatic continuum and future research should be dedicated. A regional analysis further shows that the seasonal carbon dynamics at the coast–open interface are well represented in our climatology. While our combined product is only a first step towards a true representation of both the open-ocean and the coastal-ocean air–sea CO2 flux in marine carbon budgets, we show it is a feasible task and the present data product already constitutes a valuable tool to investigate and quantify the dynamics of the air–sea CO2 exchange consistently for oceanic regions regardless of its distance to the coast. 

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3. Autonomous seawater <i>p</i>CO₂ and pH time series from 40 surface buoys and the emergence of anthropogenic trends

   https://doi.org/10.5194/essd-11-421-2019  

   Sutton, Adrienne J. ; Feely, Richard A. ; Maenner-Jones, Stacy ; Musielwicz, Sylvia ; Osborne, John ; Dietrich, Colin ; Monacci, Natalie ; Cross, Jessica ; Bott, Randy ; Kozyr, Alex ; et al ( January 2019 , Earth System Science Data)

   Abstract. Ship-based time series, some now approaching over 3 decades long, are critical climate records that have dramatically improved our ability to characterize natural and anthropogenic drivers of ocean carbon dioxide (CO2) uptake and biogeochemical processes. Advancements in autonomous marine carbon sensors and technologies over the last 2 decades have led to the expansion of observations at fixed time series sites, thereby improving the capability of characterizing sub-seasonal variability in the ocean. Here, we present a data product of 40 individual autonomous moored surface ocean pCO2 (partial pressure of CO2) time series established between 2004 and 2013, 17 also include autonomous pH measurements. These time series characterize a wide range of surface ocean carbonate conditions in different oceanic (17 sites), coastal (13 sites), and coral reef (10 sites) regimes. A time of trend emergence (ToE) methodology applied to the time series that exhibit well-constrained daily to interannual variability and an estimate of decadal variability indicates that the length of sustained observations necessary to detect statistically significant anthropogenic trends varies by marine environment. The ToE estimates for seawater pCO2 and pH range from 8 to 15 years at the open ocean sites, 16 to 41 years at the coastal sites, and 9 to 22 years at the coral reef sites. Only two open ocean pCO2 time series, Woods Hole Oceanographic Institution Hawaii Ocean Time-series Station (WHOTS) in the subtropical North Pacific and Stratus in the South Pacific gyre, have been deployed longer than the estimated trend detection time and, for these, deseasoned monthly means show estimated anthropogenic trends of 1.9±0.3 and 1.6±0.3 µatm yr−1, respectively. In the future, it is possible that updates to this product will allow for the estimation of anthropogenic trends at more sites; however, the product currently provides a valuable tool in an accessible format for evaluating climatology and natural variability of surface ocean carbonate chemistry in a variety of regions. Data are available at https://doi.org/10.7289/V5DB8043 and https://www.nodc.noaa.gov/ocads/oceans/Moorings/ndp097.html (Sutton et al., 2018). 

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4. Terrestrial exospheric dayside H-density profile at 3–15 <i>R</i>_E from UVIS/HDAC and TWINS Lyman-<i>α</i> data combined

   https://doi.org/10.5194/angeo-40-271-2022  

   Zoennchen, Jochen H. ; Connor, Hyunju K. ; Jung, Jaewoong ; Nass, Uwe ; Fahr, Hans J. ( January 2022 , Annales Geophysicae)

   Abstract. Terrestrial ecliptic dayside observations of the exospheric Lyman-α column intensity between 3–15 Earth radii (RE) by UVIS/HDAC (UVIS – ultraviolet imaging spectrograph; HDAC – hydrogen-deuterium absorptioncell) Lyman-α photometer at CASSINI have been analyzed to derive the neutral exospheric H-density profile at the Earth's ecliptic dayside in this radial range. The data were measured during CASSINI's swing-by maneuver at the Earth on 18 August 1999 and are published by Werner et al. (2004). In this study the dayside HDAC Lyman-α observations published by Werner et al. (2004) are compared to calculated Lyman-α intensities based on the 3D H-density model derived from TWINS (Two Wide-angle Imaging Neutral-atom Spectrometers) Lyman-α observations between 2008–2010 (Zoennchen et al., 2015). It was found that both Lyman-α profiles show a very similar radial dependence in particular between 3–8 RE. Between 3.0–5.5 RE impact distance Lyman-α observations of both TWINS and UVIS/HDAC exist at the ecliptic dayside. In this overlapping region the cross-calibration of the HDAC profile against the calculated TWINS profile was done, assuming that the exosphere there was similar for both due to comparable space weather conditions. As a result of the cross-calibration the conversion factor between counts per second and rayleigh, fc=3.285 counts s−1 R−1, is determined for these HDAC observations. Using this factor the radial H-density profile for the Earth's ecliptic dayside was derived from the UVIS/HDAC observations, which constrained the neutral H density there at 10 RE to a value of 35 cm−3. Furthermore, a faster radial H-density decrease was found at distances above 8 RE (≈r-3) compared to the lower distances of 3–7 RE (≈r-2.37). This increased loss of neutral H above 8 RE might indicate a higher rate of H ionization in the vicinity of the magnetopause at 9–11 RE (near subsolar point) and beyond, because of increasing charge exchange interactions of exospheric H atoms with solar wind ions outside the magnetosphere. 

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5. FLUXNET-CH₄: a global, multi-ecosystem dataset and analysis of methane seasonality from freshwater wetlands

   https://doi.org/10.5194/essd-13-3607-2021  

   Delwiche, Kyle B. ; Knox, Sara Helen ; Malhotra, Avni ; Fluet-Chouinard, Etienne ; McNicol, Gavin ; Feron, Sarah ; Ouyang, Zutao ; Papale, Dario ; Trotta, Carlo ; Canfora, Eleonora ; et al ( January 2021 , Earth System Science Data)

   null (Ed.)

   Abstract. Methane (CH4) emissions from natural landscapes constituteroughly half of global CH4 contributions to the atmosphere, yet largeuncertainties remain in the absolute magnitude and the seasonality ofemission quantities and drivers. Eddy covariance (EC) measurements ofCH4 flux are ideal for constraining ecosystem-scale CH4emissions due to quasi-continuous and high-temporal-resolution CH4flux measurements, coincident carbon dioxide, water, and energy fluxmeasurements, lack of ecosystem disturbance, and increased availability ofdatasets over the last decade. Here, we (1) describe the newly publisheddataset, FLUXNET-CH4 Version 1.0, the first open-source global dataset ofCH4 EC measurements (available athttps://fluxnet.org/data/fluxnet-ch4-community-product/, last access: 7 April 2021). FLUXNET-CH4includes half-hourly and daily gap-filled and non-gap-filled aggregatedCH4 fluxes and meteorological data from 79 sites globally: 42freshwater wetlands, 6 brackish and saline wetlands, 7 formerly drainedecosystems, 7 rice paddy sites, 2 lakes, and 15 uplands. Then, we (2) evaluate FLUXNET-CH4 representativeness for freshwater wetland coverageglobally because the majority of sites in FLUXNET-CH4 Version 1.0 arefreshwater wetlands which are a substantial source of total atmosphericCH4 emissions; and (3) we provide the first global estimates of theseasonal variability and seasonality predictors of freshwater wetlandCH4 fluxes. Our representativeness analysis suggests that thefreshwater wetland sites in the dataset cover global wetland bioclimaticattributes (encompassing energy, moisture, and vegetation-relatedparameters) in arctic, boreal, and temperate regions but only sparselycover humid tropical regions. Seasonality metrics of wetland CH4emissions vary considerably across latitudinal bands. In freshwater wetlands(except those between 20∘ S to 20∘ N) the spring onsetof elevated CH4 emissions starts 3 d earlier, and the CH4emission season lasts 4 d longer, for each degree Celsius increase in meanannual air temperature. On average, the spring onset of increasing CH4emissions lags behind soil warming by 1 month, with very few sites experiencingincreased CH4 emissions prior to the onset of soil warming. Incontrast, roughly half of these sites experience the spring onset of risingCH4 emissions prior to the spring increase in gross primaryproductivity (GPP). The timing of peak summer CH4 emissions does notcorrelate with the timing for either peak summer temperature or peak GPP.Our results provide seasonality parameters for CH4 modeling andhighlight seasonality metrics that cannot be predicted by temperature or GPP(i.e., seasonality of CH4 peak). FLUXNET-CH4 is a powerful new resourcefor diagnosing and understanding the role of terrestrial ecosystems andclimate drivers in the global CH4 cycle, and future additions of sitesin tropical ecosystems and site years of data collection will provide addedvalue to this database. All seasonality parameters are available athttps://doi.org/10.5281/zenodo.4672601 (Delwiche et al., 2021).Additionally, raw FLUXNET-CH4 data used to extract seasonality parameterscan be downloaded from https://fluxnet.org/data/fluxnet-ch4-community-product/ (last access: 7 April 2021), and a completelist of the 79 individual site data DOIs is provided in Table 2 of this paper. 

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