Description: Nitrous oxide (N2O) is a long-lived potent greenhouse gas and stratospheric ozone-depleting substance, which has been accumulating in the atmosphere since the pre-industrial period. The mole fraction of atmospheric N2O has increased by nearly 25 % from 270 parts per billion (ppb) in 1750 to 336 ppb in 2022, with the fastest annual growth rate since 1980 of more than 1.3 ppb yr-1 in both 2020 and 2021. As a core component of our global greenhouse gas assessments coordinated by the Global Carbon Project (GCP), we present a global N2O budget that incorporates both natural and anthropogenic sources and sinks, and accounts for the interactions between nitrogen additions and the biochemical processes that control N2O emissions. We use Bottom-Up (BU: inventory, statistical extrapolation of flux measurements, process-based land and ocean modelling) and Top-Down (TD: atmospheric measurement-based inversion) approaches. We provide a comprehensive quantification of global N2O sources and sinks in 21 natural and anthropogenic categories in 18 regions between 1980 and 2020. We estimate that total annual anthropogenic N2O emissions increased 40 % (or 1.9 Tg N yr-1) in the past four decades (1980–2020). Direct agricultural emissions in 2020, 3.9 Tg N yr−1 (best estimate) represent the large majority of anthropogenic emissions, followed by other direct anthropogenic sources (including ‘Fossil fuel and industry’, ‘Waste and wastewater’, and ‘Biomass burning’ (2.1 Tg N yr−1), and indirect anthropogenic sources (1.3 Tg N yr−1). For the year 2020, our best estimate of total BU emissions for natural and anthropogenic sources was 18.3 (lower-upper bounds: 10.5–27.0) Tg N yr-1, close to our TD estimate of 17.0 (16.6–17.4) Tg N yr-1. For the period 2010–2019, the annual BU decadal-average emissions for natural plus anthropogenic sources were 18.1 (10.4–25.9) Tg N yr-1 and TD emissions were 17.4 (15.8–19.20 Tg N yr-1. The once top emitter Europe has reduced its emissions since the 1980s by 31 % while those of emerging economies have grown, making China the top emitter since the 2010s. The observed atmospheric N2O concentrations in recent years have exceeded projected levels under all scenarios in the Coupled Model Intercomparison Project Phase 6 (CMIP6), underscoring the urgency to reduce anthropogenic N2O emissions. To evaluate mitigation efforts and contribute to the Global Stocktake of the United Nations Framework Convention on Climate Change, we propose establishing a global network for monitoring and modeling N2O from the surface through the stratosphere. The data presented in this work can be downloaded from https://doi.org/10.18160/RQ8P-2Z4R (Tian et al. 2023).

Description: The carbon cycle component of the newly developed Earth System Model of intermediate complexity CLIMBER-X is presented. The model represents the cycling of carbon through atmosphere, vegetation, soils, seawater and marine sediments. Exchanges of carbon with geological reservoirs occur through sediment burial, rock weathering and volcanic degassing. The state-of-the-art HAMOCC6 model is employed to simulate ocean biogeochemistry and marine sediments processes. The land model PALADYN simulates the processes related to vegetation and soil carbon dynamics, including permafrost and peatlands. The dust cycle in the model allows for an interactive determination of the input of the micro-nutrient iron into the ocean. A rock weathering scheme is implemented into the model, with the weathering rate depending on lithology, runoff and soil temperature. CLIMBER-X includes a simple representation of the methane cycle, with explicitly modelled natural emissions from land and the assumption of a constant residence time of CH4 in the atmosphere. Carbon isotopes 13C and 14C are tracked through all model compartments and provide a useful diagnostic for model-data comparison. A comprehensive evaluation of the model performance for present–day and the historical period shows that CLIMBER-X is capable of realistically reproducing the historical evolution of atmospheric CO2 and CH4, but also the spatial distribution of carbon on land and the 3D structure of biogeochemical ocean tracers. The analysis of model performance is complemented by an assessment of carbon cycle feedbacks and model sensitivities compared to state-of-the-art CMIP6 models. Enabling interactive carbon cycle in CLIMBER-X results in a relatively minor slow-down of model computational performance by ~20 %, compared to a throughput of ~10,000 simulation years per day on a single node with 16 CPUs on a high performance computer in a climate–only model setup. CLIMBER-X is therefore well suited to investigate the feedbacks between climate and the carbon cycle on temporal scales ranging from decades to 〉100,000 years.

Description: Ocean alkalinity enhancement (OAE) seeks to increase the alkalinity of seawater for carbon dioxide removal (CDR). Following numerous propositions to trial, test, or upscale OAE for CDR, multiple social considerations have begun to be identified. To ensure that OAE research is responsible (is attentive to societal priorities) and successful (does not prematurely engender widespread social rejection), it will be critical to understand how OAE might be perceived as risky or controversial and under what conditions it might be regarded by relevant social groups as most worthy of exploration. To facilitate the answering of these questions, this chapter does the following: (1) characterizes what is known to date about public perceptions of OAE, (2) provides methodological suggestions on how to conduct social science research and public engagement to accompany OAE field research, and (3) addresses how knowledge gained from social research and public engagement on OAE can be integrated into ongoing scientific, siting, and communications work.

Description: Nitrogen (N) and phosphorus (P) biogeochemical dynamics are crucial for the regulation of the terrestrial carbon cycle. In Earth system models (ESMs) the implementation of nutrient limitations has been shown to improve the carbon cycle feedback representation and, hence, the fidelity of the response of land to simulated atmospheric CO2 rise. Here we aimed to implement a terrestrial N and P cycle in an Earth system model of intermediate complexity to improve projections of future CO2 fertilization feedbacks. The N cycle is an improved version of the Wania et al. (2012) N module, with enforcement of N mass conservation and the merger with a deep land-surface and wetland module that allows for the estimation of N2O and NO fluxes. The N cycle module estimates fluxes from three organic (litter, soil organic matter and vegetation) and two inorganic ( and ) pools and accounts for inputs from biological N fixation and N deposition. The P cycle module contains the same organic pools with one inorganic P pool; it estimates influx of P from rock weathering and losses from leaching and occlusion. Two historical simulations are carried out for the different nutrient limitation setups of the model: carbon and nitrogen (CN), as well as carbon, nitrogen and phosphorus (CNP), with a baseline carbon-only simulation. The improved N cycle module now conserves mass, and the added fluxes (NO and N2O), along with the N and P pools, are within the range of other studies and literature. For the years 2001–2015 the nutrient limitation resulted in a reduction of gross primary productivity (GPP) from the carbon-only value of 143 to 130 Pg C yr−1 in the CN version and 127 Pg C yr−1 in the CNP version. This implies that the model efficiently represents a nutrient limitation over the CO2 fertilization effect. CNP simulation resulted in a reduction of 11 % of the mean GPP and a reduction of 23 % of the vegetation biomass compared to the baseline C simulation. These results are in better agreement with observations, particularly in tropical regions where P limitation is known to be important. In summary, the implementation of the N and P cycle has successfully enforced a nutrient limitation in the terrestrial system, which has now reduced the primary productivity and the capacity of land to take up atmospheric carbon, better matching observations.

Description: Ocean alkalinity enhancement (OAE) is an emerging strategy that aims to mitigate climate change by increasing the alkalinity of seawater. This approach involves increasing the alkalinity of the ocean to enhance its capacity to absorb and store carbon dioxide (CO2) from the atmosphere. This chapter presents an overview of the technical aspects associated with the full range of OAE methods being pursued and discusses implications for undertaking research on these approaches. Various methods have been developed to implement OAE, including the direct injection of alkaline liquid into the surface ocean; dispersal of alkaline particles from ships, platforms, or pipes; the addition of minerals to coastal environments; and the electrochemical removal of acid from seawater. Each method has its advantages and challenges, such as scalability, cost effectiveness, and potential environmental impacts. The choice of technique may depend on factors such as regional oceanographic conditions, alkalinity source availability, and engineering feasibility. This chapter considers electrochemical methods, the accelerated weathering of limestone, ocean liming, the creation of hydrated carbonates, and the addition of minerals to coastal environments. In each case, the technical aspects of the technologies are considered, and implications for best-practice research are drawn. The environmental and social impacts of OAE will likely depend on the specific technology and the local context in which it is deployed. Therefore, it is essential that the technical feasibility of OAE is undertaken in parallel with, and informed by, wider impact assessments. While OAE shows promise as a potential climate change mitigation strategy, it is essential to acknowledge its limitations and uncertainties. Further research and development are needed to understand the long-term effects, optimize techniques, and address potential unintended consequences. OAE should be viewed as complementary to extensive emission reductions, and its feasibility may be improved if it is operated using energy and supply chains with minimal CO2 emissions.

Description: We compare Holocene tree-cover changes in Europe derived from a transient MPI-ESM1.2 simulation with high spatial resolution LPJ-GUESS time-slice simulations and pollen-based quantitative reconstructions of tree cover based on the REVEALS model. The dynamic vegetation models and REVEALS agree with respect to the general temporal trends in tree cover for most parts of Europe, with a large tree cover during the mid-Holocene and a substantially smaller tree cover closer to the present time. However, the decrease in tree cover in REVEALS starts much earlier than in the models indicating much earlier anthropogenic deforestation than the prescribed land-use in the models. While LPJ-GUESS generally overestimates tree cover compared to the reconstructions, MPI-ESM indicates lower percentages of tree cover than REVEALS, particularly in Central Europe and the British Isles. A comparison of the simulated climate with chironomid-based climate reconstructions reveals that model-data mismatches in tree cover are in most cases not driven by biases in the climate. Instead, sensitivity experiments indicate that the model results strongly depend on the tuning of the models regarding natural disturbance regimes (e.g. fire and wind throw). The frequency and strength of disturbances are – like most of the parameters in the vegetation models – static and calibrated to modern conditions. However, these parameter values may not be valid during climate and vegetation states totally different from todays. In particular, the mid-Holocene natural forests were probably more stable and less sensitive to disturbances than present day forests that are heavily altered by human interventions. Our analysis highlights the fact that such model settings are inappropriate for palaeo-simulations and complicate model-data comparisons with additional challenges. Moreover, our study suggests that land-use is the main driver of forest decline in Europe during the mid- and late-Holocene.

Description: Carbon monoxide (CO) is an atmospheric trace gas that plays a crucial role in the oxidizing capacity of the Earth’s atmosphere. Moreover, it functions as an indirect greenhouse gas, influencing the lifetimes of potent greenhouse gases such as methane. Albeit being an overall source of atmospheric CO, the role of coastal regions in the marine cycling of CO and how its budget can be affected by anthropogenic activities, remain uncertain. Here, we present the first measurements of dissolved CO in the Ria Formosa Lagoon, an anthropogenically influenced system in southern Portugal. The dissolved CO concentrations in the surface layer ranged from 0.16 to 3.1 nmol L−1 with an average concentration of 0.75 ± 0.57 nmol L−1. The CO saturation ratio ranged from 1.7 to 32.2, indicating that the lagoon acted as a source of CO to the atmosphere in May 2021. The estimated average sea-to-air flux density was 1.53 μmol m−2 d−1, mainly fueled by CO photochemical production. Microbial consumption accounted for 83 % of the CO production, suggesting that the resulting CO emissions to the atmosphere were modulated by microbial consumption in the surface waters of the Ria Formosa Lagoon. The results from an irradiation experiment with aquaculture effluent water indicated that aquaculture facilities in the Ria Formosa Lagoon seem to be a negligible source of atmospheric CO.

Description: Carbon monoxide (CO) is an atmospheric trace gas that plays a crucial role in the oxidizing capacity of the Earth’s atmosphere. Moreover, it functions as an indirect greenhouse gas, influencing the lifetimes of potent greenhouse gases such as methane. Albeit being an overall source of atmospheric CO, the role of coastal regions in the marine cycling of CO and how its budget can be affected by anthropogenic activities, remain uncertain. Here, we present the first measurements of dissolved CO in the Ria Formosa Lagoon, an anthropogenically influenced system in southern Portugal. The dissolved CO concentrations in the surface layer ranged from 0.16 to 3.1 nmol L−1 with an average concentration of 0.75 ± 0.57 nmol L−1. The CO saturation ratio ranged from 1.7 to 32.2, indicating that the lagoon acted as a source of CO to the atmosphere in May 2021. The estimated average sea-to-air flux density was 1.53 μmol m−2 d−1, mainly fueled by CO photochemical production. Microbial consumption accounted for 83 % of the CO production, suggesting that the resulting CO emissions to the atmosphere were modulated by microbial consumption in the surface waters of the Ria Formosa Lagoon. The results from an irradiation experiment with aquaculture effluent water indicated that aquaculture facilities in the Ria Formosa Lagoon seem to be a negligible source of atmospheric CO.

Description: Ocean alkalinity enhancement (OAE) is a marine carbon dioxide removal (CDR) approach. Publicly funded research projects have begun, and philanthropic funding and start-ups are collectively pushing the field forward. This rapid progress in research activities has created an urgent need to learn if and how OAE can work at scale. The Best Practices Guide to OAE research contains 7 topics broken down into 13 chapters that compare and synthesise previously published methods and offer guidance for future research.