Description: Author Posting. © American Geophysical Union, 2021. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Journal of Geophysical Research: Oceans 126(8), (2021): e2021JC017510, https://doi.org/10.1029/2021JC017510.

Description: The air-sea exchange of oxygen (O2) is driven by changes in solubility, biological activity, and circulation. The total air-sea exchange of O2 has been shown to be closely related to the air-sea exchange of heat on seasonal timescales, with the ratio of the seasonal flux of O2 to heat varying with latitude, being higher in the extratropics and lower in the subtropics. This O2/heat ratio is both a fundamental biogeochemical property of air-sea exchange and a convenient metric for testing earth system models. Current estimates of the O2/heat flux ratio rely on sparse observations of dissolved O2, leaving it fairly unconstrained. From a model ensemble we show that the ratio of the seasonal amplitude of two atmospheric tracers, atmospheric potential oxygen (APO) and the argon-to-nitrogen ratio (Ar/O2), exhibits a close relationship to the O2/heat ratio of the extratropics (40–70°). The amplitude ratio, A APO/A ArN2, is relatively constant within the extratropics of each hemisphere due to the zonal mixing of the atmosphere. A APO/A ArN2 is not sensitive to atmospheric transport, as most of the observed spatial variability in the seasonal amplitude of δAPO is compensated by similar variations in δ(Ar/N2). From the relationship between O2/heat and A APO/A ArN2 in the model ensemble, we determine that the atmospheric observations suggest hemispherically distinct O2/heat flux ratios of 3.3 ± 0.3 and 4.7 ± 0.8 nmol J-1 between 40 and 70° in the Northern and Southern Hemispheres respectively, providing a useful constraint for O2 and heat air-sea fluxes in earth system models and observation-based data products.

Description: The recent atmospheric measurements of the Scripps program have been supported via funding from the NSF and the National Oceanographic and Atmospheric Administration (NOAA) under grants 1304270 and OAR-CIPO-2015-2004269. M. Manizza and R. F. Keeling thank NSF for financial support via the OCE-1130976 grant. M. Manizza thanks additional financial support from NSF via the ARRA OCE-0850350 grant. S. C. Doney acknowledges support from NSF PLR-1440435. Keith Rodgers acknowledges support from IBS-R028-D1. Gael Forget and the ECCO group kindly provided the ECCOv4 heat fluxes.

Description: 2022-01-22

Description: 〈jats:p〉Abstract. 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 synthesize 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 fCO2 products. The terrestrial CO2 sink (SLAND) is estimated with dynamic global vegetation models. Additional lines of evidence on land and ocean sinks are provided by atmospheric inversions, atmospheric oxygen measurements, and Earth system 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 incomplete understanding of the contemporary carbon cycle. All uncertainties are reported as ±1σ. For the year 2022, EFOS increased by 0.9 % relative to 2021, with fossil emissions at 9.9±0.5 Gt C yr−1 (10.2±0.5 Gt C yr−1 when the cement carbonation sink is not included), and ELUC was 1.2±0.7 Gt C yr−1, for a total anthropogenic CO2 emission (including the cement carbonation sink) of 11.1±0.8 Gt C yr−1 (40.7±3.2 Gt CO2 yr−1). Also, for 2022, GATM was 4.6±0.2 Gt C yr−1 (2.18±0.1 ppm yr−1; ppm denotes parts per million), SOCEAN was 2.8±0.4 Gt C yr−1, and SLAND was 3.8±0.8 Gt C yr−1, with a BIM of −0.1 Gt C yr−1 (i.e. total estimated sources marginally too low or sinks marginally too high). The global atmospheric CO2 concentration averaged over 2022 reached 417.1±0.1 ppm. Preliminary data for 2023 suggest an increase in EFOS relative to 2022 of +1.1 % (0.0 % to 2.1 %) globally and atmospheric CO2 concentration reaching 419.3 ppm, 51 % above the pre-industrial level (around 278 ppm in 1750). Overall, the mean of and trend in the components of the global carbon budget are consistently estimated over the period 1959–2022, with a near-zero overall budget imbalance, although discrepancies of up to around 1 Gt C yr−1 persist for the representation of annual to semi-decadal variability in CO2 fluxes. Comparison of estimates from multiple approaches and observations shows the following: (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 methods and data sets applied to this most recent global carbon budget as well as evolving community understanding of the global carbon cycle. The data presented in this work are available at https://doi.org/10.18160/GCP-2023 (Friedlingstein et al., 2023). 〈/jats:p〉

Description: A new, near-coastal background site was established for observations of greenhouse gases (GHGs) and atmospheric oxygen in the central Namib Desert near Gobabeb, Namibia. The location of the site was chosen to provide observations in a data-poor region in the global sampling network for GHGs. Semi-automated, continuous measurements of carbon dioxide, methane, nitrous oxide, carbon monoxide, atmospheric oxygen, and basic meteorology are made at a height of 21 m a.g.l., 50 km from the coast at the northern border of the Namib Sand Sea. Atmospheric oxygen is measured with a differential fuel cell analyzer. Carbon dioxide and methane are measured with an early-model cavity ring-down spectrometer; nitrous oxide and carbon monoxide are measured with an off-axis integrated cavity output spectrometer. Instrument-specific water corrections are employed for both instruments in lieu of drying. The representativity of the site was assessed within the context of atmospheric transport. During austral summer, strong equatorward winds are present as a result of the Hadley circulation. This brings marine boundary layer air inland to Gobabeb. In austral winter, the descending branch of the southern Hadley cell is at the same latitude as NDAO, which encourages the establishment of anticyclonic conditions over southern Africa. The variability of air mass history during this time of year is quite high, alternating between marine and terrestrial air masses, as well as air that was recently in contact with the surface and air that had descended from heights greater than 2 km. NOAA ask samples taken at Gobabeb from 1996 to the present appeared to respond to these seasonal patterns in atmospheric dynamics, when compared to other marine background sites at the same latitude as NDAO. Two years of data are presented from the observatory. Diurnal variability was noted at times for all species, particularly for atmospheric oxygen. Through stoichiometry and phasing, this was attributed primarily to the local wind system, which features a prominent sea breeze, and daily boundary layer oscillations. Large anomalies in carbon monoxide and methane were observed in the time series on a synoptic time scale, during the ascending portion of the seasonal cycle. These were attributed to an alternation between polluted air masses from the continental interior and marine boundary layer air. The continental air masses were progressively in uenced by biomass burning as the fire season developed. The concentration of re activity close to the station increased throughout the year, peaking in September, a fact re ected in the enhancement ratio of CH4 to CO. During such synoptic events the molar exchange ratio of O2 to CO2 also supported this interpretation. Finally, the NDAO time series was used to make top-down estimates of air-sea fl uxes of the main measurands from the Lüderitz and Walvis Bay upwelling cells in the Benguela Current region, during upwelling events. Flux densities were evaluated using shipboard measurements within the study area, showing good agreement with the top-down estimates. Average flux densities for CO2 were 0.450.4 µmol m-2 sec-1, -3.92.6 µmol m-2 sec-1 for O2, 6.05.0 nmol m-2 sec-1 for CH4, 0.50.4 nmol m-2 sec-1 for N2O, and 2.71.7 nmol m-2 sec-1 for CO. N2O uxes were fairly low, in accord with previous work, suggesting that the evasion of this gas from the Benguela is smaller than in other upwelling systems. Conversely, methane release was very high for the marine environment, which adds to mounting evidence of a large sedimentary source of methane in the Walvis Bay area. Carbon dioxide and oxygen uxes were substantial and probably not accounted for in current budgets.

Description: Nitrous oxide (N2O) and carbon monoxide (CO) are atmospheric trace gases which significantly influence Earth’s climate through their role as greenhouse gases. In addition, N2O is currently considered to be main ozone-depleting substance of the 21st century. Despite its importance, N2O and CO emission estimates from vast areas of the ocean are associated with large uncertainties mainly due to the lack of adequate temporal and spatial resolution. By making use of a novel technique based upon off-axis integrated cavity output spectroscopy (OA-ICOS) in combination with custom equilibration systems, we developed a method which allows measuring along-track N2O and CO in surface waters and the overlying atmosphere. Performance tests demonstrated the high stability of the analytic system, with low optimal integration times of 2 and 4 min for N2O and CO respectively, as well as detection limits 〈 40 ppt and precision better than 0.3 ppb Hz−1/2. Comparison of our method and well-established discrete methods for dissolved N2O and atmospheric CO evidenced a reliable operation of the setup in the field. The applicability of the system for continuous measurements both in research ships and vessels of opportunity is discussed in light of the results obtained during different deployments carried out in the tropical and North Atlantic.

Description: 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 synthesize data sets and methodology to quantify the five major components of the global carbon budget and their uncertainties. Fossil CO2 emissions (E-FOS) are based on energy statistics and cement production data, while emissions from land-use change (E-LUC), 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 (G(ATM)) is computed from the annual changes in concentration. The ocean CO2 sink (S-OCEAN) is estimated with global ocean biogeochemistry models and observation-based fCO(2) products. The terrestrial CO2 sink (S-LAND) is estimated with dynamic global vegetation models. Additional lines of evidence on land and ocean sinks are provided by atmospheric inversions, atmospheric oxygen measurements, and Earth system models. The resulting carbon budget imbalance (B-IM), 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 incomplete understanding of the contemporary carbon cycle. All uncertainties are reported as +/- 1 sigma. For the year 2022, E-FOS increased by 0.9% relative to 2021, with fossil emissions at 9.9 +/- 0.5 GtC yr(-1) (10.2 +/- 0.5 GtC yr(-1) when the cement carbonation sink is not included), and E-LUC was 1.2 +/- 0.7 GtC yr(-1), for a total anthropogenic CO2 emission (including the cement carbonation sink) of 11.1 +/- 0.8 GtC yr(-1) (40.7 +/- 3.2 GtCO(2) yr(-1)). Also, for 2022, G(ATM) was 4.6 +/- 0.2 GtC yr(-1) (2.18 +/- 0.1 ppm yr(-1); ppm denotes parts per million), S-OCEAN was 2.8 +/- 0.4 GtC yr(-1), and S-LAND was 3.8 +/- 0.8 GtC yr(-1), with a B-IM of 0.1 GtC yr(-1) (i.e. total estimated sources marginally too low or sinks marginally too high). The global atmospheric CO2 concentration averaged over 2022 reached 417.1 +/- 0.1 ppm. Preliminary data for 2023 suggest an increase in E-FOS relative to 2022 of +/- 1:1% (0.0% to 2.1 %) globally and atmospheric CO2 concentration reaching 419.3 ppm, 51% above the pre-industrial level (around 278 ppm in 1750). Overall, the mean of and trend in the components of the global carbon budget are consistently estimated over the period 1959-2022, with a near-zero overall budget imbalance, although discrepancies of up to around 1 Gt Cyr(-1) persist for the representation of annual to semi-decadal variability in CO2 fluxes. Comparison of estimates from multiple approaches and observations shows the following: (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 methods and data sets applied to this most recent global carbon budget as well as evolving community understanding of the global carbon cycle.