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Abstract We assess the Southern Ocean CO₂uptake (1985–2018) using data sets gathered in the REgional Carbon Cycle Assessment and Processes Project Phase 2. The Southern Ocean acted as a sink for CO₂with close agreement between simulation results from global ocean biogeochemistry models (GOBMs, 0.75 ± 0.28 PgC yr⁻¹) andpCO₂‐observation‐based products (0.73 ± 0.07 PgC yr⁻¹). This sink is only half that reported by RECCAP1 for the same region and timeframe. The present‐day net uptake is to first order a response to rising atmospheric CO₂, driving large amounts of anthropogenic CO₂(C_ant) into the ocean, thereby overcompensating the loss of natural CO₂to the atmosphere. An apparent knowledge gap is the increase of the sink since 2000, withpCO₂‐products suggesting a growth that is more than twice as strong and uncertain as that of GOBMs (0.26 ± 0.06 and 0.11 ± 0.03 Pg C yr⁻¹ decade⁻¹, respectively). This is despite nearly identicalpCO₂trends in GOBMs andpCO₂‐products when both products are compared only at the locations wherepCO₂was measured. Seasonal analyses revealed agreement in driving processes in winter with uncertainty in the magnitude of outgassing, whereas discrepancies are more fundamental in summer, when GOBMs exhibit difficulties in simulating the effects of the non‐thermal processes of biology and mixing/circulation. Ocean interior accumulation of C_antpoints to an underestimate of C_antuptake and storage in GOBMs. Future work needs to link surface fluxes and interior ocean transport, build long overdue systematic observation networks and push toward better process understanding of drivers of the carbon cycle. 

Climate change is affecting a wide range of global systems, with polar ecosystems experiencing the most rapid change. Although climate impacts affect lower-trophic-level and short-lived species most directly, it is less clear how long-lived and mobile species will respond to rapid polar warming because they may have the short-term ability to accommodate ecological disruptions while adapting to new conditions. We found that the population dynamics of an iconic and highly mobile polar-associated species are tightly coupled to Arctic prey availability and access to feeding areas. When low prey biomass coincided with high ice cover, gray whales experienced major mortality events, each reducing the population by 15 to 25%. This suggests that even mobile, long-lived species are sensitive to dynamic and changing conditions as the Arctic warms. 

Abstract. 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). 

Abstract Nitrous oxide (N₂O) is a greenhouse gas and stratospheric ozone‐depleting substance with large and growing anthropogenic emissions. Previous studies identified the influx of N₂O‐depleted air from the stratosphere to partly cause the seasonality in tropospheric N₂O (aN₂O), but other contributions remain unclear. Here, we combine surface fluxes from eight land and four ocean models from phase 2 of the Nitrogen/N₂O Model Intercomparison Project with tropospheric transport modeling to simulate aN₂O at eight remote air sampling sites for modern and pre‐industrial periods. Models show general agreement on the seasonal phasing of zonal‐average N₂O fluxes for most sites, but seasonal peak‐to‐peak amplitudes differ several‐fold across models. The modeled seasonal amplitude of surface aN₂O ranges from 0.25 to 0.80 ppb (interquartile ranges 21%–52% of median) for land, 0.14–0.25 ppb (17%–68%) for ocean, and 0.28–0.77 ppb (23%–52%) for combined flux contributions. The observed seasonal amplitude ranges from 0.34 to 1.08 ppb for these sites. The stratospheric contributions to aN₂O, inferred by the difference between the surface‐troposphere model and observations, show 16%–126% larger amplitudes and minima delayed by ∼1 month compared to Northern Hemisphere site observations. Land fluxes and their seasonal amplitude have increased since the pre‐industrial era and are projected to grow further under anthropogenic activities. Our results demonstrate the increasing importance of land fluxes for aN₂O seasonality. Considering the large model spread, in situ aN₂O observations and atmospheric transport‐chemistry models will provide opportunities for constraining terrestrial and oceanic biosphere models, critical for projecting carbon‐nitrogen cycles under ongoing global warming. 

Abstract The air‐sea exchange of oxygen (O₂) is driven by changes in solubility, biological activity, and circulation. The total air‐sea exchange of O₂has been shown to be closely related to the air‐sea exchange of heat on seasonal timescales, with the ratio of the seasonal flux of O₂to heat varying with latitude, being higher in the extratropics and lower in the subtropics. This O₂/heat ratio is both a fundamental biogeochemical property of air‐sea exchange and a convenient metric for testing earth system models. Current estimates of the O₂/heat flux ratio rely on sparse observations of dissolved O₂, leaving it fairly unconstrained. From a model ensemble we show that the ratio of the seasonal amplitude of two atmospheric tracers, atmospheric potential oxygen (APO) and the argon‐to‐nitrogen ratio (Ar/O₂), exhibits a close relationship to the O₂/heat ratio of the extratropics (40–). The amplitude ratio,/, is relatively constant within the extratropics of each hemisphere due to the zonal mixing of the atmosphere./is not sensitive to atmospheric transport, as most of the observed spatial variability in the seasonal amplitude ofAPO is compensated by similar variations in(Ar/). From the relationship between/heat and/in the model ensemble, we determine that the atmospheric observations suggest hemispherically distinct/heat flux ratios of 3.30.3 and 4.70.8 nmolbetween 40 andin the Northern and Southern Hemispheres respectively, providing a useful constraint forand heat air‐sea fluxes in earth system models and observation‐based data products.