ALBERT

Description: [1] The global-scale quantification of organic carbon (Corg) degradation pathways in marine sediments is difficult to achieve experimentally due to the limited availability of field data. In the present study, a numerical modeling approach is used as an alternative to quantify the major metabolic pathways of Corg oxidation (Cox) and associated fluxes of redox-sensitive species fluxes along a global ocean hypsometry, using the seafloor depth (SFD) as the master variable. The SFD dependency of the model parameters and forcing functions is extracted from existing empirical relationships or from the NOAA World Ocean Atlas. Results are in general agreement with estimates from the literature showing that the relative contribution of aerobic respiration to Cox increases from 〈10% at shallow SFD to 〉80% in deep-sea sediments. Sulfate reduction essentially follows an inversed SFD dependency, the other metabolic pathways (denitrification, Mn and Fe reduction) only adding minor contributions to the global-scale mineralization of Corg. The hypsometric analysis allows the establishment of relationships between the individual terminal electron acceptor (TEA) fluxes across the sediment-water interface and their respective contributions to the Corg decomposition process. On a global average, simulation results indicate that sulfate reduction is the dominant metabolic pathway and accounts for approximately 76% of the total Cox, which is higher than reported so far by other authors. The results also demonstrate the importance of bioirrigation for the assessment of global species fluxes. Especially at shallow SFD most of the TEAs enter the sediments via bioirrigation, which complicates the use of concentration profiles for the determination of total TEA fluxes by molecular diffusion. Furthermore, bioirrigation accounts for major losses of reduced species from the sediment to the water column prohibiting their reoxidation inside the sediment. As a result, the total carbon mineralization rate exceeds the total flux of oxygen into the sediment by a factor of 2 globally.

Description: A one‐dimensional reaction‐transport model is used to investigate the dynamics of methane gas in coastal sediments in response to intra‐annual variations in temperature and pressure. The model is applied to data from two shallow water sites in Eckernförde Bay (Germany) characterized by low and high rates of upward fluid advection. At both sites, organic matter is buried below the sulfate‐reducing zone to the methanogenic zone at sufficiently high rates to allow supersaturation of the pore water with dissolved methane and to form a free methane gas phase. The methane solubility concentration varies by similar magnitudes at both study sites in response to bottom water temperature changes and leads to pronounced peaks in the gas volume fraction in autumn when the methanic zone temperature is at a maximum. Yearly hydrostatic pressure variations have comparatively negligible effects on methane solubility. Field data suggest that no free gas escapes to the water column at any time of the year. Although the existence of gas migration cannot be substantiated by direct observation, a speculative mechanism for slow moving gas is proposed here. The model results reveal that free gas migrating upward into the undersaturated pore water will completely dissolve and subsequently be consumed above the free gas depth (FGD) by anaerobic oxidation of methane (AOM). This microbially mediated process maintains methane undersaturation above the FGD. Although the complexities introduced by seasonal changes in temperature lead to different seasonal trends for the depth‐integrated AOM rates and the FGD, both sites adhere to previously developed prognostic indicators for methane fluxes based on the FGD.

Description: The coastal ocean contributes to regulating atmospheric greenhouse gas concentrations by taking up carbon dioxide (CO2) and releasing nitrous oxide (N2O) and methane (CH4). In this second phase of the Regional Carbon Cycle Assessment and Processes (RECCAP2), we quantify global coastal ocean fluxes of CO2, N2O and CH4 using an ensemble of global gap-filled observation-based products and ocean biogeochemical models. The global coastal ocean is a net sink of CO2 in both observational products and models, but the magnitude of the median net global coastal uptake is similar to 60% larger in models (-0.72 vs. -0.44 PgC year-1, 1998-2018, coastal ocean extending to 300 km offshore or 1,000 m isobath with area of 77 million km2). We attribute most of this model-product difference to the seasonality in sea surface CO2 partial pressure at mid- and high-latitudes, where models simulate stronger winter CO2 uptake. The coastal ocean CO2 sink has increased in the past decades but the available time-resolving observation-based products and models show large discrepancies in the magnitude of this increase. The global coastal ocean is a major source of N2O (+0.70 PgCO2-e year-1 in observational product and +0.54 PgCO2-e year-1 in model median) and CH4 (+0.21 PgCO2-e year-1 in observational product), which offsets a substantial proportion of the coastal CO2 uptake in the net radiative balance (30%-60% in CO2-equivalents), highlighting the importance of considering the three greenhouse gases when examining the influence of the coastal ocean on climate. The coastal ocean regulates greenhouse gases. It acts as a sink of carbon dioxide (CO2) but also releases nitrous oxide (N2O) and methane (CH4) into the atmosphere. This synthesis contributes to the second phase of the Regional Carbon Cycle Assessment and Processes (RECCAP2) and provides a comprehensive view of the coastal air-sea fluxes of these three greenhouse gases at the global scale. We use a multi-faceted approach combining gap-filled observation-based products and ocean biogeochemical models. We show that the global coastal ocean is a net sink of CO2 in both observational products and models, but the coastal uptake of CO2 is similar to 60% larger in models than in observation-based products due to model-product differences in seasonality. The coastal CO2 sink is strengthening but the magnitude of this strengthening is poorly constrained. We also find that the coastal emissions of N2O and CH4 counteract a substantial part of the effect of coastal CO2 uptake in the atmospheric radiative balance (by 30%-60% in CO2-equivalents), highlighting the need to consider these three gases together to understand the influence of the coastal ocean on climate. We synthesize air-sea fluxes of CO2, nitrous oxide and methane in the global coastal ocean using observation-based products and ocean models The coastal ocean CO2 sink is 60% larger in ocean models than in observation-based products due to systematic differences in seasonality Coastal nitrous oxide and methane emissions offset 30%-60% of the CO2 coastal uptake in the net radiative balance

Description: © The Author(s), 2015. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Earth System Science Data 7 (2015): 47-85, doi:10.5194/essd-7-47-2015.

Description: 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, consistency within and among components, alongside methodology and data limitations. CO2 emissions from fossil fuel combustion and cement production (EFF) are based on energy statistics and cement production data, respectively, 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 (2004–2013), EFF was 8.9 ± 0.4 GtC yr−1, ELUC 0.9 ± 0.5 GtC yr−1, GATM 4.3 ± 0.1 GtC yr−1, SOCEAN 2.6 ± 0.5 GtC yr−1, and SLAND 2.9 ± 0.8 GtC yr−1. For year 2013 alone, EFF grew to 9.9 ± 0.5 GtC yr−1, 2.3% above 2012, continuing the growth trend in these emissions, ELUC was 0.9 ± 0.5 GtC yr−1, GATM was 5.4 ± 0.2 GtC yr−1, SOCEAN was 2.9 ± 0.5 GtC yr−1, and SLAND was 2.5 ± 0.9 GtC yr−1. GATM was high in 2013, reflecting a steady increase in EFF and smaller and opposite changes between SOCEAN and SLAND compared to the past decade (2004–2013). The global atmospheric CO2 concentration reached 395.31 ± 0.10 ppm averaged over 2013. We estimate that EFF will increase by 2.5% (1.3–3.5%) to 10.1 ± 0.6 GtC in 2014 (37.0 ± 2.2 GtCO2 yr−1), 65% above emissions in 1990, based on projections of world gross domestic product and recent changes in the carbon intensity of the global economy. From this projection of EFF and assumed constant ELUC for 2014, cumulative emissions of CO2 will reach about 545 ± 55 GtC (2000 ± 200 GtCO2) for 1870–2014, about 75% from EFF and 25% from ELUC. This paper documents changes in the methods and data sets used in this new carbon budget compared with previous publications of this living data set (Le Quéré et al., 2013, 2014). All observations presented here can be downloaded from the Carbon Dioxide Information Analysis Center (doi:10.3334/CDIAC/GCP_2014).

Description: NERC provided funding to C. Le Quéré, R. Moriarty, and the GCP though their International Opportunities Fund specifically to support this publication (NE/103002X/1), and to U. Schuster through UKOARP (NE/H017046/1). G. P. Peters and R. M. Andrews were supported by the Norwegian Research Council (236296). T. A. Boden was supported by US Department of Energy, Office of Science, Biological and Environmental Research (BER) programmes under US Department of Energy contract DEAC05- 00OR22725. Y. Bozec was supported by Region Bretagne, CG29, and INSU (LEFE/MERMEX) for CARBORHONE cruises. J. G. Canadell and M. R. Raupach were supported by the Australian Climate Change Science Programme. M. Hoppema received ICOSD funding through the German Federal Ministry of Education and Research (BMBF) to the AWI (01 LK 1224I). J. I. House was supported by a Leverhulme Early Career Fellowship. A. K. Jain was supported by the US National Science Foundation (NSF AGS 12-43071) the US Department of Energy, Office of Science, and BER programmes (DOE DE-SC0006706) and the NASA LCLUC programme (NASA NNX14AD94G). E. Kato was supported by the Environment Research and Technology Development Fund (S-10) of the Ministry of Environment of Japan. C. Koven was supported by the Director, Office of Science, Office of Biological and Environmental Research, of the US Department of Energy under contract no. DE-AC02-05CH11231 as part of their Regional and Global Climate Modeling Program. I. D. Lima was supported by the U.S. National Science Foundation (NSF AGS-1048827). N. Metzl was supported by Institut National des Sciences de l’Univers (INSU) and Institut Paul Emile Victor (IPEV) for OISO cruises. A. Olsen was supported by the Centre for Climate Dynamics at the Bjerknes Centre for Climate Research. J. E. Salisbury was supported by grants from NOAA/NASA. T. Steinhoff was supported by ICOS-D (BMBF FK 01LK1101C). B. D. Stocker was supported by the Swiss National Science Foundation and FP7 funding through project EMBRACE (282672). A. J. Sutton was supported by NOAA. T. Takahashi was supported by grants from NOAA and the Comer Education and Science Foundation. B. Tilbrook was supported by the Australian Department of the Environment and the Integrated Marine Observing System. A.Wiltshire was supported by the Joint UK DECC/Defra Met Office Hadley Centre Climate Programme (GA01101). P. Ciais,W. Peters, C. Le Quére, P. Regnier, and U. Schuster were supported by the EU FP7 through project GEOCarbon (283080). A. Arneth, P. Ciais, S. Sitch, and A. Wiltshire were supported by COMBINE (226520). V. Kitidis, M. Hoppema, N. Metzl, C. Le Quéré, U. Schuster, J. Schwiger, J. Segschneider, and T. Steinhoff were supported by the EU FP7 through project CARBOCHANGE (264879). A. Arnet, P. Friedlingstein, B. Poulter, and S. Sitch were supported by the EU FP7 through projects LUC4C (GA603542). P. Friedlingstein was also supported by EMBRACE (GA282672). F. Chevallier and G. R. van der Werf were supported by the EU FP7 through project MACC-II (283576).