Tatiana Ilyina

Carbon-concentration and carbon-climate feedbacks in CMIP5 Earth System Models

AbstractThe magnitude and evolution of parameters that characterize feedbacks in the coupled carbon–climate system are compared across nine Earth system models (ESMs). The analysis is based on results from biogeochemically, radiatively, and fully coupled simulations in which CO2 increases at a rate of 1% yr−1. These simulations are part of phase 5 of the Coupled Model Intercomparison Project (CMIP5). The CO2 fluxes between the atmosphere and underlying land and ocean respond to changes in atmospheric CO2 concentration and to changes in temperature and other climate variables. The carbon–concentration and carbon–climate feedback parameters characterize the response of the CO2 flux between the atmosphere and the underlying surface to these changes. Feedback parameters are calculated using two different approaches. The two approaches are equivalent and either may be used to calculate the contribution of the feedback terms to diagnosed cumulative emissions. The contribution of carbon–concentration feedback to...

Nonlinearity of Ocean Carbon Cycle Feedbacks in CMIP5 Earth System Models

Carbon cycle feedbacks are usually categorized into carbon–concentration and carbon–climate feedbacks, which arise owing to increasing atmospheric CO2 concentration and changing physical climate. Both feedbacks are often assumedtooperateindependently:thatis,thetotalfeedbackcanbeexpressed asthesumoftwoindependentcarbon fluxes that are functions of atmospheric CO2 and climate change, respectively. For phase 5 of the Coupled Model Intercomparison Project (CMIP5), radiatively and biogeochemically coupled simulations have been undertaken to better understand carbon cycle feedback processes. Results show that the sum of total ocean carbon uptake in the radiatively and biogeochemically coupled experiments is consistently larger by 19–58 petagrams of carbon (Pg C) than the uptake found in the fully coupled model runs. This nonlinearity is small compared to the total ocean carbon uptake (533–676PgC), but it is of the same order as the carbon–climate feedback. The weakening of ocean circulation and mixing with climate change makes the largest contribution to the nonlinear carbon cycle response since carbon transport to depth is suppressed in the fully relative to the biogeochemically coupled simulations, while the radiatively coupled experiment mainly measures the loss of near-surface carbon owing to warming of the ocean. Sea ice retreat and seawater carbon chemistry contribute less to the simulated nonlinearity. The authors’ results indicate thatestimatesoftheocean carbon–climate feedback derived from‘‘warming only’’ (radiativelycoupled)simulations may underestimate the reduction of ocean carbon uptake in a warm climate high CO2 world.

Assessing the potential of calcium‐based artificial ocean alkalinization to mitigate rising atmospheric CO2 and ocean acidification

Enhancement of ocean alkalinity using calcium compounds, e.g., lime has been proposed to mitigate further increase of atmospheric CO2 and ocean acidification due to anthropogenic CO2 emissions. Using a global model, we show that such alkalinization has the potential to preserve pH and the saturation state of carbonate minerals at close to today’s values. Effects of alkalinization persist after termination: Atmospheric CO2 and pH do not return to unmitigated levels. Only scenarios in which large amounts of alkalinity (i.e., in a ratio of 2:1 with respect to emitted CO2) are added over large ocean areas can boost oceanic CO2 uptake sufficiently to avoid further ocean acidification on the global scale, thereby elevating some key biogeochemical parameters, e.g., pH significantly above preindustrial levels. Smaller-scale alkalinization could counteract ocean acidification on a subregional or even local scale, e.g., in upwelling systems. The decrease of atmospheric CO2 would then be a small side effect.

Towards real-time verification of CO2 emissions

The Paris Agreement has increased the incentive to verify reported anthropogenic carbon dioxide emissions with independent Earth system observations. Reliable verification requires a step change in our understanding of carbon cycle variability.

Detection and attribution of climate change signal in ocean wind waves

AbstractSurface waves in the ocean respond to variability and changes of climate. Observations and modeling studies indicate trends in wave height over the past decades. Nevertheless, it is currently impossible to discern whether these trends are the result of climate variability or change. The output of an Earth system model (EC-EARTH) produced within phase 5 of the Coupled Model Intercomparison Project (CMIP5) is used here to force a global Wave Model (WAM) in order to study the response of waves to different climate regimes. A control simulation was run to determine the natural (unforced) model variability. A simplified fingerprint approach was used to calculate positive and negative limits of natural variability for wind speed and significant wave height, which were then compared to different (forced) climate regimes over the historical period (1850–2010) and in the future climate change scenario RCP8.5 (2010–2100). Detectable climate change signals were found in the current decade (2010–20) in the No...

Impacts of artificial ocean alkalinization on the carbon cycle and climate in Earth system simulations

Using the state-of-the-art emissions-driven Max Planck Institute Earth system model, we explore the impacts of artificial ocean alkalinization (AOA) with a scenario based on the Representative Concentration Pathway (RCP) framework. Addition of 114 Pmol of alkalinity to the surface ocean stabilizes atmospheric CO2 concentration to RCP4.5 levels under RCP8.5 emissions. This scenario removes 940 GtC from the atmosphere and mitigates 1.5 K of global warming within this century. The climate adjusts to the lower CO2 concentration preventing the loss of sea ice and high sea level rise. Seawater pH and the carbonate saturation state (Ω) rise substantially above levels of the current decade. Pronounced differences in regional sensitivities to AOA are projected, with the Arctic Ocean and tropical oceans emerging as hot spots for biogeochemical changes induced by AOA. Thus, the CO2 mitigation potential of AOA comes at a price of an unprecedented ocean biogeochemistry perturbation with unknown ecological consequences.

Decadal predictions of the North Atlantic CO2 uptake

As a major CO2 sink, the North Atlantic, especially its subpolar gyre region, is essential for the global carbon cycle. Decadal fluctuations of CO2 uptake in the North Atlantic subpolar gyre region are associated with the evolution of the North Atlantic Oscillation, the Atlantic meridional overturning circulation, ocean mixing and sea surface temperature anomalies. While variations in the physical state of the ocean can be predicted several years in advance by initialization of Earth system models, predictability of CO2 uptake has remained unexplored. Here we investigate the predictability of CO2 uptake variations by initialization of the MPI-ESM decadal prediction system. We find large multi-year variability in oceanic CO2 uptake and demonstrate that its potential predictive skill in the western subpolar gyre region is up to 4–7 years. The predictive skill is mainly maintained in winter and is attributed to the improved physical state of the ocean.

Evaluating CMIP5 ocean biogeochemistry and Southern Ocean carbon uptake using atmospheric potential oxygen: Present-day performance and future projection

Observed seasonal cycles in atmospheric potential oxygen (APO~O2 + 1.1 CO2) were used to evaluate eight ocean biogeochemistry models from the Coupled Model Intercomparison Project (CMIP5). Model APO seasonal cycles were computed from the CMIP5 air-sea O2 and CO2 fluxes and compared to observations at three Southern Hemisphere monitoring sites. Four of the models captured either the observed APO seasonal amplitude or phasing relatively well, while the other four did not. Many models had an unrealistic seasonal phasing or amplitude of the CO2 flux, which in turn influenced APO. By 2100 under RCP8.5, the models projected little change in the O2 component of APO but large changes in the seasonality of the CO2 component associatedwith ocean acidification. Themodels with poorer performance on present-day APO tended to project larger net carbon uptake in the Southern Ocean, both today and in 2100.

Net primary productivity estimates and environmental variables in the Arctic Ocean: An assessment of coupled physical-biogeochemical models

The relative skill of 21 regional and global biogeochemical models was assessed in terms of how well the models reproduced observed net primary productivity (NPP) and environmental variables such as nitrate concentration (NO3), mixed layer depth (MLD), euphotic layer depth (Zeu), and sea ice concentration, by comparing results against a newly updated, quality-controlled in situ NPP database for the Arctic Ocean (1959–2011). The models broadly captured the spatial features of integrated NPP (iNPP) on a pan-Arctic scale. Most models underestimated iNPP by varying degrees in spite of overestimating surface NO3, MLD, and Zeu throughout the regions. Among the models, iNPP exhibited little difference over sea ice condition (ice-free versus ice-influenced) and bottom depth (shelf versus deep ocean). The models performed relatively well for the most recent decade and toward the end of Arctic summer. In the Barents and Greenland Seas, regional model skill of surface NO3 was best associated with how well MLD was reproduced. Regionally, iNPP was relatively well simulated in the Beaufort Sea and the central Arctic Basin, where in situ NPP is low and nutrients are mostly depleted. Models performed less well at simulating iNPP in the Greenland and Chukchi Seas, despite the higher model skill in MLD and sea ice concentration, respectively. iNPP model skill was constrained by different factors in different Arctic Ocean regions. Our study suggests that better parameterization of biological and ecological microbial rates (phytoplankton growth and zooplankton grazing) are needed for improved Arctic Ocean biogeochemical modeling.

Quantifying and Comparing Effects of Climate Engineering Methods on the Earth System

To contribute to a quantitative comparison of climate engineering (CE) methods, we assess atmosphere-, ocean-, and land-based CE measures with respect to Earth system effects consistently within one comprehensive model. We use the Max Planck Institute Earth System Model (MPI-ESM) with prognostic carbon cycle to compare solar radiation management (SRM) by stratospheric sulfur injection and two carbon dioxide removal methods: afforestation and ocean alkalinization. The CE model experiments are designed to offset the effect of fossil-fuel burning on global mean surface air temperature under the RCP8.5 scenario to follow or get closer to the RCP4.5 scenario. Our results show the importance of feedbacks in the CE effects. For example, as a response to SRM the land carbon uptake is enhanced by 92Gt by the year 2100 compared to the reference RCP8.5 scenario due to reduced soil respiration thus reducing atmospheric CO2. Furthermore, we show that normalizations allow for a better comparability of different CE methods. For example, we find that due to compensating processes such as biogeophysical effects of afforestation more carbon needs to be removed from the atmosphere by afforestation than by alkalinization to reach the same global warming reduction. Overall, we illustrate how different CE methods affect the components of the Earth system; we identify challenges arising in a CE comparison, and thereby contribute to developing a framework for a comparative assessment of CE.