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Accurate assessment of anthropogenic carbon dioxide (CO2) emissions and their redistribution among the atmosphere, ocean, and terrestrial biosphere is important to better understand the global carbon cycle, support the development of climate policies, and project future climate change. Here we describe data sets and a methodology to quantify all major components of the global carbon budget, including their uncertainties, based on the combination of a range of data, algorithms, statistics, and model estimates and their interpretation by a broad scientific community. We discuss changes compared to previous estimates as well as consistency within and among components, alongside methodology and data limitations. CO2 emissions from fossil fuels and industry (EFF) are based on energy statistics and cement production data, while emissions from land-use change (ELUC), mainly deforestation, are based on combined evidence from land-cover-change data, fire activity associated with deforestation, and models. The global atmospheric CO2 concentration is measured directly and its rate of growth (GATM) is computed from the annual changes in concentration. The mean ocean CO2 sink (SOCEAN) is based on observations from the 1990s, while the annual anomalies and trends are estimated with ocean models. The variability in SOCEAN is evaluated with data products based on surveys of ocean CO2 measurements. The global residual terrestrial CO2 sink (SLAND) is estimated by the difference of the other terms of the global carbon budget and compared to results of independent dynamic global vegetation models forced by observed climate, CO2, and land-cover change (some including nitrogen–carbon interactions). We compare the mean land and ocean fluxes and their variability to estimates from three atmospheric inverse methods for three broad latitude bands. All uncertainties are reported as ±1σ, reflecting the current capacity to characterise the annual estimates of each component of the global carbon budget. For the last decade available (2005–2014), EFF was 9.0 ± 0.5 GtC yr−1, ELUC was 0.9 ± 0.5 GtC yr−1, GATM was 4.4 ± 0.1 GtC yr−1, SOCEAN was 2.6 ± 0.5 GtC yr−1, and SLAND was 3.0 ± 0.8 GtC yr−1. For the year 2014 alone, EFF grew to 9.8 ± 0.5 GtC yr−1, 0.6 % above 2013, continuing the growth trend in these emissions, albeit at a slower rate compared to the average growth of 2.2 % yr−1 that took place during 2005–2014. Also, for 2014, ELUC was 1.1 ± 0.5 GtC yr−1, GATM was 3.9 ± 0.2 GtC yr−1, SOCEAN was 2.9 ± 0.5 GtC yr−1, and SLAND was 4.1 ± 0.9 GtC yr−1. GATM was lower in 2014 compared to the past decade (2005–2014), reflecting a larger SLAND for that year. The global atmospheric CO2 concentration reached 397.15 ± 0.10 ppm averaged over 2014. For 2015, preliminary data indicate that the growth in EFF will be near or slightly below zero, with a projection of −0.6 [range of −1.6 to +0.5] %, based on national emissions projections for China and the USA, and projections of gross domestic product corrected for recent changes in the carbon intensity of the global economy for the rest of the world. From this projection of EFF and assumed constant ELUC for 2015, cumulative emissions of CO2 will reach about 555 ± 55 GtC (2035 ± 205 GtCO2) for 1870–2015, about 75 % from EFF and 25 % from ELUC. This living data update documents changes in the methods and data sets used in this new carbon budget compared with previous publications of this data set (Le Quéré et al., 2015, 2014, 2013). All observations presented here can be downloaded from the Carbon Dioxide Information Analysis Center (doi:10.3334/CDIAC/GCP_2015).

The Southern Ocean is highly under-sampled for the purpose of assessing total carbon uptake and its variability. Since this region dominates the mean global ocean sink for anthropogenic carbon, understanding temporal change is critical. Underway measurements of pCO2 collected as part of the Drake Passage Time-series (DPT) program that began in 2002 inform our understanding of seasonally changing air–sea gradients in pCO2, and by inference the carbon flux in this region. Here, we utilize availablepCO2 observations to evaluate how the seasonal cycle, interannual variability, and long-term trends in surface ocean pCO2 in the Drake Passage region compare to that of the broader subpolar Southern Ocean. Our results indicate that the Drake Passage is representative of the broader region in both seasonality and long-term pCO2 trends, as evident through the agreement of timing and amplitude of seasonal cycles as well as trend magnitudes both seasonally and annually. The high temporal density of sampling by the DPT is critical to constraining estimates of the seasonal cycle of surface pCO2 in this region, as winter data remain sparse in areas outside of the Drake Passage. An increase in winter data would aid in reduction of uncertainty levels. On average over the period 2002–2016, data show that carbon uptake has strengthened with annual surface ocean pCO2 trends in the Drake Passage and the broader subpolar Southern Ocean less than the global atmospheric trend. Analysis of spatial correlation shows Drake Passage pCO2 to be representative ofpCO2 and its variability up to several hundred kilometers away from the region. We also compare DPT data from 2016 and 2017 to contemporaneous pCO2 estimates from autonomous biogeochemical floats deployed as part of the Southern Ocean Carbon and Climate Observations and Modeling project (SOCCOM) so as to highlight the opportunity for evaluating data collected on autonomous observational platforms. Though SOCCOM floats sparsely sample the Drake Passage region for 2016–2017 compared to the Drake Passage Time-series, their pCO2 estimates fall within the range of underway observations given the uncertainty on the estimates. Going forward, continuation of the Drake Passage Time-series will reduce uncertainties in Southern Ocean carbon uptake seasonality, variability, and trends, and provide an invaluable independent dataset for post-deployment assessment of sensors on autonomous floats. Together, these datasets will vastly increase our ability to monitor change in the ocean carbon sink.

The late Taro Takahashi (Lamont-Doherty Earth Observatory (LDEO), Columbia University) and colleagues provided the first near-global monthly air–sea CO2 flux climatology in Takahashi et al. (1997), based on available surface water partial pressure of CO2 measurements. This product has been a benchmark for uptake of CO2 in the ocean. Several versions have been provided since, with improvements in procedures and large increases in observations, culminating in the authoritative assessment in Takahashi et al. (2009a, b). Here we provide and document the last iteration using a greatly increased dataset (SOCATv2022) and determining fluxes using air–sea partial pressure differences as a climatological reference for the period 1980–2021 (Fay et al., 2023, 10.25921/295g-sn13). The resulting net flux for the open ocean region is estimated as -1.79±0.7 Pg C yr-1, which compares well with other global mean flux estimates. While global flux results are consistent, differences in regional means and seasonal amplitudes are discussed. Consistent with other studies, we find the largest differences in the data-sparse southeast Pacific and Southern Ocean.

Antarctic pack ice is inhabited by a diverse and active microbial community reliant on nutrients for growth. Seeking patterns and overlooked processes, we performed a large-scale compilation of macro-nutrient data (hereafter termed nutrients) in Antarctic pack ice (306 ice-cores collected from 19 research cruises). Dissolved inorganic nitrogen and silicic acid concentrations change with time, as expected from a seasonally productive ecosystem. In winter, salinity-normalized nitrate and silicic acid concentrations (C*) in sea ice are close to seawater concentrations (Cw), indicating little or no biological activity. In spring, nitrate and silicic acid concentrations become partially depleted with respect to seawater (C* < Cw), commensurate with the seasonal build-up of ice microalgae promoted by increased insolation. Stronger and earlier nitrate than silicic acid consumption suggests that a significant fraction of the primary productivity in sea ice is sustained by flagellates. By both consuming and producing ammonium and nitrite, the microbial community maintains these nutrients at relatively low concentrations in spring. With the decrease in insolation beginning in late summer, dissolved inorganic nitrogen and silicic acid concentrations increase, indicating imbalance between their production (increasing or unchanged) and consumption (decreasing) in sea ice. Unlike the depleted concentrations of both nitrate and silicic acid from spring to summer, phosphate accumulates in sea ice (C* > Cw). The phosphate excess could be explained by a greater allocation to phosphorus-rich biomolecules during ice algal blooms coupled with convective loss of excess dissolved nitrogen, preferential remineralization of phosphorus, and/or phosphate adsorption onto metal-organic complexes. Ammonium also appears to be efficiently adsorbed onto organic matter, with likely consequences to nitrogen mobility and availability. This dataset supports the view that the sea ice microbial community is highly efficient at processing nutrients but with a dynamic quite different from that in oceanic surface waters calling for focused future investigations.

[...]while deeply involved in his professional capacity, Clarke remained a devoted family man, and one readily sensed the reciprocal love and support of his wife, Muriel, and Neil, Joy, Stuart, and Grant, whose partners were warmly welcomed, as well as the gift of grandchildren.

To examine the importance of hunting mortality in the population dynamics of waterfowl in southwestern Australia, we estimated survival and recovery rates of 19,523 Pacific black ducks (Anas superciliosa) and 2,487 grey teal (A. gibberifrons) banded in 1968-76 and recovered by 1978. Both species showed strong evidence of year-to-year variation in survival rates, which averaged 63 ± 4(SE)% and 56 ± 6% for adult and young Pacific black ducks, respectively, and 55 ± 17% for adult grey teal. First-year recovery rates indicated the average annual hunting mortality over 6 years for Pacific black ducks and grey teal exposed to heavy hunting pressure was 23 ± 2% and 17 ± 2%, respectively. Hunting mortality was 9% in 1 year for Pacific black ducks exposed to light hunting. Estimates of mortality rate on opening day of hunting seasons at a site of intense hunting varied between 7 and 20% for Pacific black ducks and 5 and 16% for grey teal. In an intensively hunted waterfowl population in southwestern Australia, nearly 60% of all mortality of Pacific black ducks and 40% of grey teal mortality resulted from hunting. Hunting probably caused <25% of mortality in most parts of southwestern Australia, however, and there was no evidence of hunting reducing survival rates.