Abstract We assess the detectability of COVID‐like emissions reductions in global atmospheric CO2concentrations using a suite of large ensembles conducted with an Earth system model. We find a unique fingerprint of COVID in the simulated growth rate of CO2sampled at the locations of surface measurement sites. Negative anomalies in growth rates persist from January 2020 through December 2021, reaching a maximum in February 2021. However, this fingerprint is not formally detectable unless we force the model with unrealistically large emissions reductions (2 or 4 times the observed reductions). Internal variability and carbon‐concentration feedbacks obscure the detectability of short‐term emission reductions in atmospheric CO2. COVID‐driven changes in the simulated, column‐averaged dry air mole fractions of CO2are eclipsed by large internal variability. Carbon‐concentration feedbacks begin to operate almost immediately after the emissions reduction; these feedbacks reduce the emissions‐driven signal in the atmosphere carbon reservoir and further confound signal detection.
more »
« less
The Ocean Carbon Response to COVID‐Related Emissions Reductions
Abstract The decline in global emissions of carbon dioxide due to the COVID‐19 pandemic provides a unique opportunity to investigate the sensitivity of the global carbon cycle and climate system to emissions reductions. Recent efforts to study the response to these emissions declines has not addressed their impact on the ocean, yet ocean carbon absorption is particularly susceptible to changing atmospheric carbon concentrations. Here, we use ensembles of simulations conducted with an Earth system model to explore the potential detection of COVID‐related emissions reductions in the partial pressure difference in carbon dioxide between the surface ocean and overlying atmosphere (ΔpCO2), a quantity that is regularly measured. We find a unique fingerprint in global‐scale ΔpCO2that is attributable to COVID, though the fingerprint is difficult to detect in individual model realizations unless we force the model with a scenario that has four times the observed emissions reduction.
more »
« less
- PAR ID:
- 10402859
- Publisher / Repository:
- DOI PREFIX: 10.1029
- Date Published:
- Journal Name:
- Geophysical Research Letters
- Volume:
- 48
- Issue:
- 6
- ISSN:
- 0094-8276
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
-
Scenarios to stabilize global climate and meet international climate agreements require rapid reductions in human carbon dioxide (CO2) emissions, often augmented by substantial carbon dioxide removal (CDR) from the atmosphere. While some ocean-based removal techniques show potential promise as part of a broader CDR and decarbonization portfolio, no marine approach is ready yet for deployment at scale because of gaps in both scientific and engineering knowledge. Marine CDR spans a wide range of biotic and abiotic methods, with both common and technique-specific limitations. Further targeted research is needed on CDR efficacy, permanence, and additionality as well as on robust validation methods—measurement, monitoring, reporting, and verification—that are essential to demonstrate the safe removal and long-term storage of CO2. Engineering studies are needed on constraints including scalability, costs, resource inputs, energy demands, and technical readiness. Research on possible co-benefits, ocean acidification effects, environmental and social impacts, and governance is also required.more » « less
-
Abstract The ocean has absorbed about 25% of the carbon emitted by humans to date. To better predict how much climate will change, it is critical to understand how this ocean carbon sink will respond to future emissions. Here, we examine the ocean carbon sink response to low emission (SSP1-1.9, SSP1-2.6), intermediate emission (SSP2-4.5, SSP5-3.4-OS), and high emission (SSP5-8.5) scenarios in CMIP6 Earth System Models and in MAGICC7, a reduced-complexity climate carbon system model. From 2020–2100, the trajectory of the global-mean sink approximately parallels the trajectory of anthropogenic emissions. With increasing cumulative emissions during this century (SSP5-8.5 and SSP2-4.5), the cumulative ocean carbon sink absorbs 20%–30% of cumulative emissions since 2015. In scenarios where emissions decline, the ocean absorbs an increasingly large proportion of emissions (up to 120% of cumulative emissions since 2015). Despite similar responses in all models, there remains substantial quantitative spread in estimates of the cumulative sink through 2100 within each scenario, up to 50 PgC in CMIP6 and 120 PgC in the MAGICC7 ensemble. We demonstrate that for all but SSP1-2.6, approximately half of this future spread can be eliminated if model results are adjusted to agree with modern observation-based estimates. Considering the spatial distribution of air-sea CO2fluxes in CMIP6, we find significant zonal-mean divergence from the suite of newly-available observation-based constraints. We conclude that a significant portion of future ocean carbon sink uncertainty is attributable to modern-day errors in the mean state of air-sea CO2fluxes, which in turn are associated with model representations of ocean physics and biogeochemistry. Bringing models into agreement with modern observation-based estimates at regional to global scales can substantially reduce uncertainty in future role of the ocean in absorbing anthropogenic CO2from the atmosphere and mitigating climate change.more » « less
-
Abstract Oceanic absorption of atmospheric carbon dioxide (CO2) is expected to slow down under increasing anthropogenic emissions; however, the driving mechanisms and rates of change remain uncertain, limiting our ability to project long‐term changes in climate. Using an Earth system simulation, we show that the uptake of anthropogenic carbon will slow in the next three centuries via reductions in surface alkalinity. Warming and associated changes in precipitation and evaporation intensify density stratification of the upper ocean, inhibiting the transport of alkaline water from the deep. The effect of these changes is amplified threefold by reduced carbonate buffering, making alkalinity a dominant control on CO2uptake on multi‐century timescales. Our simulation reveals a previously unknown alkalinity‐climate feedback loop, amplifying multi‐century warming under high emission trajectories.more » « less
-
Abstract Large Igneous Province (LIP) eruptions are thought to have driven environmental and climate change over wide temporal scales ranging from a few to thousands of years. Since the radiative effects and atmospheric lifetime of carbon dioxide (CO2, warming) and sulfur dioxide (SO2, cooling) are very different, the conventional assumption has been to analyze the effects of CO2and SO2emissions separately and add them together afterward. In this study, we test this assumption by analyzing the joint effect of CO2and SO2on the marine carbonate cycle using a biogeochemical carbon cycle box model (Long‐term Ocean‐atmosphere‐Sediment CArbon cycle Reservoir Model). By performing model runs with very fine temporal resolution (∼0.1‐year timestep), we analyze the effects of LIP carbon and sulfur gas emissions on timescales ranging from an individual eruption (hundreds to thousands of years) to the entire long‐term carbon cycle (>100,000 years). We find that, contrary to previous work, sulfur emissions have significant long‐term (>1,000 years) effects on the marine carbon cycle (dissolved inorganic carbon, pH, alkalinity, and carbonate compensation depth). This is due to two processes: the strongly temperature‐dependent equilibrium coefficients for marine carbonate chemistry and the few thousand‐year timescale for ocean overturning circulation. Thus, the effects of volcanic sulfur are not simply additive to the impact of carbon emissions. We develop a causal mechanistic framework to visualize the feedbacks associated with combined carbon and sulfur emissions and the associated timescales. Our results provide a new perspective for understanding the complex feedback mechanisms controlling the environmental effects of large volcanic eruptions over Earth history.more » « less
An official website of the United States government
