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This dataset includes surface underway chemical, meteorological and physical data collected from Autonomous Surface Vehicle (ASV) Saildrone 1038 (EXPOCODE 316420220616) in the Indian Ocean, Southern Ocean from 2022-06-16 to 2022-07-26. These data include xCO2 SW (wet) - mole fraction of CO2 in air in equilibrium with the seawater at sea surface temperature and measured humidity; H2O SW - Mole fraction of H2O in air from equilibrator; xCO2 Air (wet) - Mole fraction of CO2 in air from airblock, 0.67m (26") above the sea surface at measured humidity; H2O Air - Mole fraction of H2O in air from airblock, 0.67m (26") above the sea surface; Atmospheric pressure at the airblock, 0.67m (26") above the sea surface; Atmospheric pressure at the airblock, 0.67m (26") above the sea surface; Temperature of the Infrared Licor 820 in degrees Celsius; MAPCO2 %O2 - The percent oxygen of the surface seawater divided by the percent oxygen of the atmosphere at 0.67m (26") above the sea surface; Sea Surface Temperature; Sea Surface Salinity; xCO2 SW (dry) - Mole fraction of CO2 in air in equilibrium with the seawater at sea surface temperature (dry air); xCO2 Air (dry) - Mole fraction of CO2 in air at the airblock, 0.67m (26") above the sea surface (dry air); fCO2 SW (sat) - Fugacity of CO2 in air in equilibrium with the seawater at sea surface temperature (100% humidity); fCO2 Air (sat) - Fugacity of CO2 in air at the airblock, 0.67m (26") above the sea surface (100% humidity); dfCO2 - Difference of the fugacity of the CO2 in seawater and the fugacity of the CO2 in air (fCO2 SW - fCO2 Air); pCO2 SW (wet) - Partial Pressure of CO2 in air in equilibrium with the seawater at sea surface temperature (100% humidity); pCO2 Air (wet) - Partial Pressure of CO2 in air at the airblock, 0.67m (26") above the sea surface (100% humidity); dpCO2 - Difference of the partial pressure of CO2 in seawater and air (pCO2 SW - pCO2 Air; pH of Seawater (total scale). The Autonomous Surface Vehicle CO2 (ASVCO2) instruments used to collect these data include Bubble type equilibrator for autonomous carbon dioxide (CO2) measurement, Carbon dioxide (CO2) gas analyzer, Humidity Sensor, and oxygen meter. 

This dataset includes surface underway chemical, meteorological and physical data collected from Autonomous Surface Vehicle (ASV) Saildrone 1039 (EXPOCODE 316420220901) in the Indian Ocean, Southern Ocean from 2022-09-01 to 2023-04-27. These data include xCO2 SW (wet) - mole fraction of CO2 in air in equilibrium with the seawater at sea surface temperature and measured humidity; H2O SW - Mole fraction of H2O in air from equilibrator; xCO2 Air (wet) - Mole fraction of CO2 in air from airblock, 0.67m (26") above the sea surface at measured humidity; H2O Air - Mole fraction of H2O in air from airblock, 0.67m (26") above the sea surface; Atmospheric pressure at the airblock, 0.67m (26") above the sea surface; Atmospheric pressure at the airblock, 0.67m (26") above the sea surface; Temperature of the Infrared Licor 820 in degrees Celsius; MAPCO2 %O2 - The percent oxygen of the surface seawater divided by the percent oxygen of the atmosphere at 0.67m (26") above the sea surface; Sea Surface Temperature; Sea Surface Salinity; xCO2 SW (dry) - Mole fraction of CO2 in air in equilibrium with the seawater at sea surface temperature (dry air); xCO2 Air (dry) - Mole fraction of CO2 in air at the airblock, 0.67m (26") above the sea surface (dry air); fCO2 SW (sat) - Fugacity of CO2 in air in equilibrium with the seawater at sea surface temperature (100% humidity); fCO2 Air (sat) - Fugacity of CO2 in air at the airblock, 0.67m (26") above the sea surface (100% humidity); dfCO2 - Difference of the fugacity of the CO2 in seawater and the fugacity of the CO2 in air (fCO2 SW - fCO2 Air); pCO2 SW (wet) - Partial Pressure of CO2 in air in equilibrium with the seawater at sea surface temperature (100% humidity); pCO2 Air (wet) - Partial Pressure of CO2 in air at the airblock, 0.67m (26") above the sea surface (100% humidity); dpCO2 - Difference of the partial pressure of CO2 in seawater and air (pCO2 SW - pCO2 Air; pH of Seawater (total scale). The Autonomous Surface Vehicle CO2 (ASVCO2) instruments used to collect these data include Bubble type equilibrator for autonomous carbon dioxide (CO2) measurement, Carbon dioxide (CO2) gas analyzer, Humidity Sensor, and oxygen meter. 

Global climate is regulated by the ocean, which stores, releases, and transports large amounts of mass, heat, carbon, and oxygen. Understanding, monitoring, and predicting the exchanges of these quantities across the ocean’s surface, their interactions with the atmosphere, and their horizontal and vertical pathways through the global oceans, are key for advancing fundamental knowledge and improving forecasts and longer-term projections of climate, weather, and ocean ecosystems. The existing global observing system provides immense value for science and society in this regard by supplying the data essential for these advancements. The tropical ocean observing system in particular has been developed over decades, motivated in large part by the far-reaching and complex global impacts of tropical climate variability and change. However, changes in observing needs and priorities, new challenges associated with climate change, and advances in observing technologies demand periodic evaluations to ensure that stakeholders’ needs are met. Previous reviews and assessments of the tropical observing system have focused separately on individual basins and their associated observing needs. Here we provide a broader perspective covering the tropical observing system as a whole. Common gaps, needs, and recommendations are identified, and interbasin differences driven by socioeconomic disparities are discussed, building on the concept of an integrated pantropical observing system. Finally, recommendations for improved observations of tropical basin interactions, through oceanic and atmospheric pathways, are presented, emphasizing the benefits that can be achieved through closer interbasin coordination and international partnerships. 

Abstract A budget approach is used to disentangle drivers of the seasonal mixed layer carbon cycle at Station ALOHA (A Long‐term Oligotrophic Habitat Assessment) in the North Pacific Subtropical Gyre (NPSG). The budget utilizes data from the WHOTS (Woods Hole—Hawaii Ocean Time‐series Site) mooring, and the ship‐based Hawai'i Ocean Time‐series (HOT) in the NPSG, a region of significant oceanic carbon uptake. Parsing the carbon variations into process components allows an assessment of both the proportional contributions of mixed layer carbon drivers and the seasonal interplay of drawdown and supply from different processes. Annual net community production reported here is at the lower end of previously published data, while net community calcification estimates are 4‐ to 7‐fold higher than available sediment trap data, the only other estimate of calcium carbonate export at this location. Although the observed seasonal cycle in dissolved inorganic carbon in the NPSG has a relatively small amplitude, larger fluxes offset each other over an average year. Major supply comes from physical transport, especially lateral eddy transport throughout the year and entrainment in the winter, offset by biological carbon uptake in the spring. Gas exchange plays a smaller role, supplying carbon to the surface ocean between Dec‐May and outgassing in Jul‐Oct. Evaporation‐precipitation (E‐P) is variable with precipitation prevailing in the first half and evaporation in the second half of the year. The observed total alkalinity signal is largely governed by E‐P with a somewhat stronger net calcification signal in the wintertime. 

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 datasets and methodologies 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) 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 global net uptake of CO2 by the ocean (SOCEAN, called the ocean sink) is estimated with global ocean biogeochemistry models and observation-based fCO2 products (fCO2 is the fugacity of CO2). The global net uptake of CO2 by the land (SLAND, called the land sink) 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 sum of all sources and sinks results in the carbon budget imbalance (BIM), a measure of imperfect data and incomplete understanding of the contemporary carbon cycle. All uncertainties are reported as ±1σ. For the year 2023, EFOS increased by 1.3 % relative to 2022, with fossil emissions at 10.1 ± 0.5 GtC yr−1 (10.3 ± 0.5 GtC yr−1 when the cement carbonation sink is not included), and ELUC was 1.0 ± 0.7 GtC yr−1, for a total anthropogenic CO2 emission (including the cement carbonation sink) of 11.1 ± 0.9 GtC yr−1 (40.6 ± 3.2 GtCO2 yr−1). Also, for 2023, GATM was 5.9 ± 0.2 GtC yr−1 (2.79 ± 0.1 ppm yr−1; ppm denotes parts per million), SOCEAN was 2.9 ± 0.4 GtC yr−1, and SLAND was 2.3 ± 1.0 GtC yr−1, with a near-zero BIM (−0.02 GtC yr−1). The global atmospheric CO2 concentration averaged over 2023 reached 419.31 ± 0.1 ppm. Preliminary data for 2024 suggest an increase in EFOS relative to 2023 of +0.8 % (−0.2 % to 1.7 %) globally and an atmospheric CO2 concentration increase by 2.87 ppm, reaching 422.45 ppm, 52 % 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 1959–2023, with a near-zero overall budget imbalance, although discrepancies of up to around 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 the following: (1) a persistent large uncertainty in the estimate of land-use change emissions, (2) 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 mean ocean sink. This living-data update documents changes in methods and datasets 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-2024 (Friedlingstein et al., 2024). 

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). 

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). 

Abstract The Blob was the early manifestation of the Northeast Pacific marine heat wave from 2013 to 2016. While the upper ocean temperature in the Blob has been well described, the impacts on marine biogeochemistry have not been fully studied. Here, we characterize and develop understanding of Eastern North Pacific upper ocean biogeochemical properties during the Winter of 2013–2014 using in situ observations, an observation‐based product, and reconstructions from a collection of ocean models. We find that the Blob is associated with significant upper ocean biogeochemical anomalies: A 5% increase in aragonite saturation state (temporary reprieve of ocean acidification) and a 3% decrease in oxygen concentration (enhanced deoxygenation). Anomalous advection and mixing drive the aragonite saturation anomaly, while anomalous heating and air‐sea gas exchange drive the oxygen anomaly. Marine heatwaves do not necessarily serve as an analog for future change as they may enhance or mitigate long‐term trends.