Low terrestrial carbon storage at the Last Glacial Maximum: constraints from multi-proxy data

Past changes in the inventory of carbon stored in vegetation and soils remain uncertain. Earlier studies inferred the increase in the land carbon inventory (Δland) between the Last Glacial Maximum (LGM) and the preindustrial period (PI) based on marine and atmospheric stable carbon isotope reconstructions, with recent estimates yielding 300–400&thinsp;GtC. Surprisingly, however, earlier studies considered a mass balance for the ocean–atmosphere–land biosphere system only. Notably, these studies neglect carbon exchange with marine sediments, weathering–burial flux imbalances, and the influence of the transient deglacial reorganization on the isotopic budgets. We show this simplification to significantly reduce Δland in simulations using the Bern3D Earth System Model of Intermediate Complexity v.2.0s. We constrain Δland to ∼850&thinsp;GtC (median estimate; 450 to 1250&thinsp;GtC ±1SD) by using reconstructed changes in atmospheric δ13C, marine δ13C, deep Pacific carbonate ion concentration, and atmospheric CO2 as observational targets in a Monte Carlo ensemble with half a million members. It is highly unlikely that the land carbon inventory was larger at LGM than PI. Sensitivities of the target variables to changes in individual deglacial carbon cycle processes are established from transient factorial simulations with the Bern3D model. These are used in the Monte Carlo ensemble and provide forcing–response relationships for future model–model and model–data comparisons. Our study demonstrates the importance of ocean–sediment interactions and burial as well as weathering fluxes involving marine organic matter to explain deglacial change and suggests a major upward revision of earlier isotope-based estimates of Δland.</p

Is there warming in the pipeline? A multi-model analysis of the Zero Emissions Commitment from CO₂

The Zero Emissions Commitment (ZEC) is the change in global mean temperature expected to occur following the cessation of net CO2 emissions and as such is a critical parameter for calculating the remaining carbon budget. The Zero Emissions Commitment Model Intercomparison Project (ZECMIP) was established to gain a better understanding of the potential magnitude and sign of ZEC, in addition to the processes that underlie this metric. A total of 18 Earth system models of both full and intermediate complexity participated in ZECMIP. All models conducted an experiment where atmospheric CO2 concentration increases exponentially until 1000 PgC has been emitted. Thereafter emissions are set to zero and models are configured to allow free evolution of atmospheric CO2 concentration. Many models conducted additional second-priority simulations with different cumulative emission totals and an alternative idealized emissions pathway with a gradual transition to zero emissions. The inter-model range of ZEC 50 years after emissions cease for the 1000 PgC experiment is −0.36 to 0.29 ∘C, with a model ensemble mean of −0.07 ∘C, median of −0.05 ∘C, and standard deviation of 0.19 ∘C. Models exhibit a wide variety of behaviours after emissions cease, with some models continuing to warm for decades to millennia and others cooling substantially. Analysis shows that both the carbon uptake by the ocean and the terrestrial biosphere are important for counteracting the warming effect from the reduction in ocean heat uptake in the decades after emissions cease. This warming effect is difficult to constrain due to high uncertainty in the efficacy of ocean heat uptake. Overall, the most likely value of ZEC on multi-decadal timescales is close to zero, consistent with previous model experiments and simple theory

Reviews and syntheses: Abrupt ocean biogeochemical change under human-made climatic forcing – warming, acidification, and deoxygenation

Abrupt changes in ocean biogeochemical variables occur as a result of human-induced climate forcing as well as those which are more gradual and occur over longer timescales. These abrupt changes have not yet been identified and quantified to the same extent as the more gradual ones. We review and synthesise abrupt changes in ocean biogeochemistry under human-induced climatic forcing. We specifically address the ocean carbon and oxygen cycles because the related processes of acidification and deoxygenation provide important ecosystem hazards. Since biogeochemical cycles depend also on the physical environment, we also describe the relevant changes in warming, circulation, and sea ice. We include an overview of the reversibility or irreversibility of abrupt marine biogeochemical changes. Important implications of abrupt biogeochemical changes for ecosystems are also discussed. We conclude that there is evidence for increasing occurrence and extent of abrupt changes in ocean biogeochemistry as a consequence of rising greenhouse gas emissions

Global nitrous oxide budget (1980--2020)

Nitrous oxide (N2O) is a long-lived potent greenhouse gas and stratospheric ozone-depleting substance that has been accumulating in the atmosphere since the preindustrial period. The mole fraction of atmospheric N2O has increased by nearly 25 % from 270 ppb (parts per billion) 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. According to the Sixth Assessment Report of the Intergovernmental Panel on Climate Change (IPCC AR6), the relative contribution of N2O to the total enhanced effective radiative forcing of greenhouse gases was 6.4 % for 1750–2022. As a core component of our global greenhouse gas assessments coordinated by the Global Carbon Project (GCP), our global N2O budget incorporates both natural and anthropogenic sources and sinks and accounts for the interactions between nitrogen additions and the biogeochemical processes that control N2O emissions. We use bottom-up (BU: inventory, statistical extrapolation of flux measurements, and process-based land and ocean modeling) 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 have increased 40 % (or 1.9 Tg N yr−1) in the past 4 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 18.5 (lower–upper bounds: 10.6–27.0) Tg N yr−1, close to our TD estimate of 17.0 (16.6–17.4) Tg N yr−1. For the 2010–2019 period, the annual BU decadal-average emissions for both natural and anthropogenic sources were 18.2 (10.6–25.9) 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 by 31 % since the 1980s, 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 importance of reducing anthropogenic N2O emissions. To evaluate mitigation efforts and contribute to the Global Stocktake of the United Nations Framework Convention on Climate Change, we propose the establishment of a global network for monitoring and modeling N2O from the surface through to the stratosphere. The data presented in this work can be downloaded from https://doi.org/10.18160/RQ8P-2Z4R (Tian et al., 2023)

Rejuvenating the ocean: mean ocean radiocarbon, CO₂ release, and radiocarbon budget closure across the last deglaciation

Radiocarbon is a tracer that provides unique insights into the ocean's ability to sequester CO2 from the atmosphere. While spatial patterns of radiocarbon in the ocean interior can indicate the vectors and timescales for carbon transport through the ocean, estimates of the global average ocean–atmosphere radiocarbon age offset (B-Atm) place constraints on the closure of the global carbon cycle. Here, we apply a Bayesian interpolation method to compiled B-Atm data to generate global interpolated fields and mean ocean B-Atm estimates for a suite of time slices across the last deglaciation. The compiled data and interpolations confirm a stepwise and spatially heterogeneous “rejuvenation” of the ocean, suggesting that carbon was released to the atmosphere through two swings of a “ventilation seesaw” operating between the North Atlantic and both the Southern Ocean and the North Pacific. Sensitivity tests using the Bern3D model of intermediate complexity demonstrate that a portion of the reconstructed deglacial B-Atm changes may reflect “phase-attenuation” biases that are unrelated to ocean ventilation and that arise from independent atmospheric radiocarbon dynamics instead. A deglacial minimum in B-Atm offsets during the Bølling–Allerød could partly reflect such a bias. However, the sensitivity tests further demonstrate that when correcting for such biases, ocean “ventilation” could still account for at least one-third of deglacial atmospheric CO2 rise. This contribution to CO2 rise appears to have continued through the Younger Dryas, though much of the impact was likely achieved by the end of the Bølling–Allerød, indicating a key role for marine carbon cycle adjustment early in the deglacial process. Our global average B-Atm estimates place further new constraints on the long-standing mystery of global radiocarbon budget closure across the last deglaciation and suggest that glacial radiocarbon production levels are likely underestimated on average by existing reconstructions.</p

Palaeomagnetism for chronologies of recent alpine lake sediments: successes and limits

Chronologies of lake-sediment records covering the last centuries to millennia are usually based on both short-lived radio nuclides and radio carbon dating. However, beyond the range of short-lived radio nuclides, age model accuracy often suffers from large radio carbon uncertainties. For high-altitude records, this issue is even more prominent as terrestrial plant fragments for radio carbon dating are often lacking due to the sparse vegetation in such environments. In this study, we evaluate the potential of the geomagnetic field secular variations as a complementary tool to establish more robust age–depth relationships. Our palaeomagnetic study, applied to five high-altitude lakes from the western European Alps, first shows that recent unconsolidated sediments can carry stable remanent magnetization. The analysis of the magnetic parameters indicates that low-coercivity

Palaeomagnetism for chronologies of recent alpine lake sediments: successes and limits

International audienc

Mechanisms of millennial-scale atmospheric CO<inf>2</inf> change in numerical model simulations

Numerical models are important tools for understanding the processes and feedbacks in the Earth system, including those involving changes in atmospheric CO2 (CO2,atm) concentrations. Here, we compile 55 published model studies (consisting of 778 individual simulations) that assess the impact of six forcing mechanisms on millennial-scale CO2,atm variations: changes in freshwater supply to the North Atlantic and Southern Ocean, the strength and position of the southern-hemisphere westerlies, Antarctic sea ice extent, and aeolian dust fluxes. We generally find agreement on the direction of simulated CO2,atm change across simulations, but the amplitude of change is inconsistent, primarily due to the different complexities of the model representation of Earth system processes. When freshwater is added to the North Atlantic, a reduced Atlantic Meridional Overturning Circulation (AMOC) is generally accompanied by an increase in Southern Ocean- and Pacific overturning, reduced Antarctic sea ice extent, spatially varying export production, and changes in carbon storage in the Atlantic (rising), in other ocean basins (generally decreasing) and on land (more varied). Positive or negative CO2,atm changes are simulated during AMOC minima due to a spatially and temporally varying dominance of individual terrestrial and oceanic drivers (and compensating effects between them) across the different models. In contrast, AMOC recoveries are often accompanied by rising CO2,atm levels, which are mostly driven by ocean carbon release (albeit from different regions). The magnitude of simulated CO2,atm rise broadly scales with the duration of the AMOC perturbation (i.e., the stadial length). When freshwater is added to the Southern Ocean, reduced deep-ocean ventilation drives a CO2,atm drop via reduced carbon release from the Southern Ocean. Although the impacts of shifted southern-hemisphere westerlies are inconsistent across model simulations, their intensification raises CO2,atm via enhanced Southern Ocean Ekman pumping. Increased supply of aeolian dust to the ocean, and thus iron fertilisation of marine productivity, consistently lowers modelled CO2,atm concentrations via more efficient nutrient utilisation. The magnitude of CO2,atm change in response to dust flux variations, however, largely depends on the complexity of models' marine ecosystem and iron cycle. This especially applies to simulations forced by Antarctic sea ice changes, in which the direction of simulated CO2,atm change varies greatly across model hierarchies. Our compilation highlights that no single (forcing) mechanism can explain observed past millennial-scale CO2,atm variability, and identifies important future needs in coupled carbon cycle-climate modelling to better understand the mechanisms governing CO2,atm changes in the past.Includes NERC funding

Global nitrous oxide budget (1980–2020)

Nitrous oxide (N₂O) is a long-lived potent greenhouse gas and stratospheric ozone-depleting substance that has been accumulating in the atmosphere since the preindustrial period. The mole fraction of atmospheric N₂O has increased by nearly 25 % from 270 ppb (parts per billion) in 1750 to 336 ppb in 2022, with the fastest annual growth rate since 1980 of more than 1.3 ppb yrˉ¹ in both 2020 and 2021. According to the Sixth Assessment Report of the Intergovernmental Panel on Climate Change (IPCC AR6), the relative contribution of N₂O to the total enhanced effective radiative forcing of greenhouse gases was 6.4 % for 1750–2022. As a core component of our global greenhouse gas assessments coordinated by the Global Carbon Project (GCP), our global N₂O budget incorporates both natural and anthropogenic sources and sinks and accounts for the interactions between nitrogen additions and the biogeochemical processes that control N₂O emissions. We use bottom-up (BU: inventory, statistical extrapolation of flux measurements, and process-based land and ocean modeling) 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 have increased 40 % (or 1.9 Tg N yrˉ¹) in the past 4 decades (1980–2020). Direct agricultural emissions in 2020 (3.9 Tg N yrˉ¹, 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 yrˉ¹), and indirect anthropogenic sources (1.3 Tg N yrˉ¹) . For the year 2020, our best estimate of total BU emissions for natural and anthropogenic sources was 18.5 (lower–upper bounds: 10.6–27.0) Tg N yrˉ¹, close to our TD estimate of 17.0 (16.6–17.4) Tg N yrˉ¹. For the 2010–2019 period, the annual BU decadal-average emissions for both natural and anthropogenic sources were 18.2 (10.6–25.9) Tg N yrˉ¹ and TD emissions were 17.4 (15.8–19.20) Tg N yrˉ¹. The once top emitter Europe has reduced its emissions by 31 % since the 1980s, 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 importance of reducing anthropogenic N₂O emissions. To evaluate mitigation efforts and contribute to the Global Stocktake of the United Nations Framework Convention on Climate Change, we propose the establishment of a global network for monitoring and modeling N₂O from the surface through to the stratosphere. The data presented in this work can be downloaded from https://doi.org/10.18160/RQ8P-2Z4R (Tian et al., 2023)