Engineering topics

Tilmes, Simone

Publications and source records attributed to Tilmes, Simone.

At least 37 records · Page 2

DOE OSTI2020

Characterization of organic aerosol across the global remote troposphere: a comparison of ATom measurements and global chemistry models

The spatial distribution and properties of submicron organic aerosol (OA) are among the key sources of uncertainty in our understanding of aerosol effects on climate. Uncertainties are particularly large over remote regions of the free troposphere and Southern Ocean, where very few data have been available and where OA predictions from AeroCom Phase II global models span 2 to 3 orders of magnitude, greatly exceeding the model spread over source regions. The (nearly) pole-to-pole vertical distribution of non-refractory aerosols was measured with an aerosol mass spectrometer onboard the NASA DC-8 aircraft as part of the Atmospheric Tomography (ATom) mission during the Northern Hemisphere summer (August 2016) and winter (February 2017). This study presents the first extensive characterization of OA mass concentrations and their level of oxidation in the remote atmosphere. OA and sulfate are the major contributors by mass to submicron aerosols in the remote troposphere, together with sea salt in the marine boundary layer. Sulfate was dominant in the lower stratosphere. OA concentrations have a strong seasonal and zonal variability, with the highest levels measured in the lower troposphere in the summer and over the regions influenced by biomass burning from Africa (up to 10 µg sm -3 ). Lower concentrations (~0.1–0.3 µg sm -3 ) are observed in the northern middle and high latitudes and very low concentrations (<0.1 µg sm -3 ) in the southern middle and high latitudes. The ATom dataset is used to evaluate predictions of eight current global chemistry models that implement a variety of commonly used representations of OA sources and chemistry, as well as of the AeroCom-II ensemble. The current model ensemble captures the average vertical and spatial distribution of measured OA concentrations, and the spread of the individual models remains within a factor of 5. These results are significantly improved over the AeroCom-II model ensemble, which shows large overestimations over these regions. However, some of the improved agreement with observations occurs for the wrong reasons, as models have the tendency to greatly overestimate the primary OA fraction and underestimate the secondary fraction. Measured OA in the remote free troposphere is highly oxygenated, with organic aerosol to organic carbon (OA/OC) ratios of ~2.2–2.8, and is 30 %–60 % more oxygenated than in current models, which can lead to significant errors in OA concentrations. The model–measurement comparisons presented here support the concept of a more dynamic OA system as proposed by Hodzic et al. (2016), with enhanced removal of primary OA and a stronger production of secondary OA in global models needed to provide better agreement with observations.

54 ENVIRONMENTAL SCIENCES↗

DOE OSTI2019

Seasonal Injection Strategies for Stratospheric Aerosol Geoengineering

Simulations of stratospheric aerosol geoengineering have typically considered injections at a constant rate over the entire year. However, the seasonal variability of both sunlight and the stratospheric circulation suggests seasonally-dependent injection strategies. In this work, we simulated single point injections of the same amount of SO 2 in each of the four seasons and at five different latitudes (30S, 15S, Equator, 15N, 30N), 5 km above the tropopause. Our findings suggest that injecting only during one season reduces the amount of SO 2 needed to achieve a certain aerosol optical depth (AOD), thus potentially reducing some of the side-effects of geoengineering. We find, in particular, that injections at 15N or 15S in spring of the corresponding hemisphere results in the largest reductions in incoming solar radiation. Compared to annual injections, by injecting in the different seasons we identify additional distinct spatiotemporal AOD patterns, thanks to seasonal differences in the stratospheric circulation.

58 GEOSCIENCES↗

DOE OSTI2019

Evaluating the Relationship between Interannual Variations in the Antarctic Ozone Hole and Southern Hemisphere Surface Climate in Chemistry–Climate Models

Studies have recently reported statistically significant relationships between observed year-to-year spring Antarctic ozone variability and the Southern Hemisphere annular mode and surface temperatures in spring–summer. This study reported herein investigates whether current chemistry–climate models (CCMs) can capture these relationships, in particular, the connection between November total column ozone (TCO) and Australian summer surface temperatures, where years with anomalously high TCO over the Antarctic polar cap tend to be followed by warmer summers. The interannual ozone–temperature teleconnection is examined over the historical period in the observations and simulations from the Whole Atmosphere Community Climate Model (WACCM) and nine other models participating in the Chemistry–Climate Model Initiative (CCMI). There is a systematic difference between the WACCM experiments forced with prescribed observed sea surface temperatures (SSTs) and those with an interactive ocean. Strong correlations between TCO and Australian temperatures are only obtained for the uncoupled experiment, suggesting that the SSTs could be important for driving both variations in Australian temperatures and the ozone hole, with no causal link between the two. Other CCMI models also tend to capture this relationship with more fidelity when driven by observed SSTs, although additional research and targeted modeling experiments are required to determine causality and further explore the role of model biases and observational uncertainty. The results indicate that CCMs can reproduce the relationship between spring ozone and summer Australian climate reported in observational studies, suggesting that incorporating ozone variability could improve seasonal predictions; however, more work is required to understand the difference between the coupled and uncoupled simulations.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

NASA NTRS2019

Large-Scale Transport into the Arctic: The Roles of the Midlatitude Jet and the Hadley Cell

Transport from the Northern Hemisphere (NH) midlatitudes to the Arctic plays a crucial role in determining the abundance of trace gases and aerosols that are important to Arctic climate via impacts on radiation and chemistry. Here we examine this transport using an idealized tracer with a fixed lifetime and predominantly midlatitude land-based sources in models participating in the Chemistry Climate Model Initiative (CCMI). We show that there is a 25%-45% difference in the Arctic concentrations of this tracer among the models. This spread is correlated with the spread in the location of the Pacific jet, as well as the spread in the location of the Hadley Cell (HC) edge, which varies consistently with jet latitude. Our results suggest that it is likely that the HC-related zonal-mean meridional transport rather than the jet-related eddy mixing is the major contributor to the inter-model spread in the transport of land-based tracers into the Arctic. Specifically, in models with a more northern jet, the HC generally extends further north and the tracer source region is mostly covered by surface southward flow associated with the lower branch of the HC, resulting in less efficient transport poleward to the Arctic. During boreal summer, there are poleward biases in jet location in free-running models, and these models likely underestimate the rate of transport into the Arctic. Models using specified dynamics do not have biases in the jet location, but do have biases in the surface meridional flow, which may result in differences in transport into the Arctic. In addition to the land-based tracer, the midlatitude-to-Arctic transport is further examined by another idealized tracer with zonally uniform sources. With equal sources from both land and ocean, the inter-model spread of this zonally uniform tracer is more related to variations in parameterized convection over oceans rather than variations in HC extent, particularly during boreal winter. This suggests that transport of land-based and oceanic tracers or aerosols towards the Arctic differs in pathways and therefore their corresponding inter-model variabilities result from different physical processes.

chemistry climate models↗

DOE OSTI2019

Timescale for Detecting the Climate Response to Stratospheric Aerosol Geoengineering

Stratospheric aerosol geoengineering could be used to maintain global mean temperature despite increased atmospheric greenhouse gas (GHG) concentrations, for example to meet a 1.5C or 2C target. While this might reduce many climate change impacts, the resulting climate would not be the same as one with the same global mean temperature due to lower GHG concentrations. The primary question we consider is how long it would take to detect these differences in a hypothetical deployment. We use a recently available 20-member ensemble of stratospheric sulfate aerosol geoengineering simulations in which SO2 is injected at four different latitudes to maintain not just the global mean temperature, but also the interhemispheric and equator-to-pole gradients. This multiple-latitude strategy better matches the climate changes from increased GHG, while the ensemble allows us both to estimate residual differences even when they are small compared to natural variability, and to estimate the statistics of variability. We first construct a linear emulator to predict the model responses for different scenarios. Under an RCP4.5 scenario in which geoengineering maintains a 1.5C target (providing end-of-century cooling of 1.7C), the change in global mean precipitation is projected to have a signal-to-noise ratio (SNR) greater than one after only 11 years. However, in this scenario, the projected temperature and precipitation changes at a grid-scale are typically small enough that in many regions this threshold is still not reached by the end of this century. These results provide some context for the projected magnitude of climate-changes associated with a limited deployment of stratospheric aerosol cooling.

42 ENGINEERING↗

DOE OSTI2018

CESM1(WACCM) Stratospheric Aerosol Geoengineering Large Ensemble Project

This paper describes the stratospheric aerosol geoengineering large ensemble (GLENS) project, which promotes the use of an unique model dataset, performed with Community Earth System Model, using the Whole Atmosphere Community Climate Model as its atmospheric component (CESM1(WACCM)), to investigate global and regional impacts of geoengineering. The performed simulations target multiple simultaneous climate goals unlike many earlier studies that targeted globally averaged surface temperature. This strategic approach is expected to reduce some of the previously found adverse effects of stratospheric aerosol geoengineering, including uneven cooling between the poles and equator and shifts in tropical precipitation. An ensemble of 20 members allows the identification of forced changes in global and regional climate variables in the coupled atmosphere, land, sea-ice, and ocean system in the presence of internal variability. Here, we invite the broader community to perform in-depth analysis of climate related impacts and to identify processes that lead to changes in the climate system as the result of a strategic application of stratospheric aerosol geoengineering. (Capsule Summary) A community project that enables analysis of robust global and regional changes resulting from strategic stratospheric aerosol geoengineering in the presence of internal climate variability.

58 GEOSCIENCES↗

DOE OSTI2018

Response of Surface Ultraviolet and Visible Radiation to Stratospheric SO 2 Injections

Climate modification by stratospheric SO 2 injections, to form sulfate aerosols, may alter the spectral and angular distributions of the solar ultraviolet and visible radiation that reach the Earth’s surface, with potential consequences to environmental photobiology and photochemistry. We used modeling results from the CESM1(WACCM) stratospheric aerosol geoengineering large ensemble (GLENS) project, following the RCP8.5 emission scenario, and one geoengineering experiment with SO 2 injections in the stratosphere, designed to keep surface temperatures at 2020 levels. Zonally and monthly averaged vertical profiles of O 3 , SO 2 , and sulfate aerosols, at 30 N and 70 N, served as input into a radiative transfer model, to compute biologically active irradiances for DNA damage ( i DNA ), UV index (UVI), photosynthetically active radiation (PAR), and two key tropospheric photodissociation coefficients ( j O1D for O 3 + hν (λ < 330 nm) → O( 1 D) + O 2 ; and j NO2 for NO 2 + hν (λ < 420 nm) → O( 3 P) + NO). We show that the geoengineering scenario is accompanied by substantial reductions in UV radiation. For example, comparing March 2080 to March 2020, i DNA decreased by 25% to 29% in the subtropics (30 N) and by 26% to 33% in the polar regions (70 N); UVI decreased by 19% to 20% at 30 N and 23% to 26% at 70 N; and j O1D decreased by 22% to 24% at 30 N and 35% to 40% at 70 N, with comparable contributions from sulfate scattering and stratospheric O 3 recovery. Different responses were found for processes that depend on longer UV and visible wavelengths, as these are minimally affected by ozone; PAR and j NO2 were only slightly lower (9–12%) at 30 N, but much lower at 70 N (35–40%). Similar reductions were estimated for other months (June, September, and December). Large increases in the PAR diffuse-direct ratio occurred in agreement with previous studies. Absorption by SO 2 gas had a small (~1%) effect on j O1D , i DNA , and UVI, and no effect on j NO2 and PAR.

42 ENGINEERING↗

DOE OSTI2018

Long-range transport impacts on surface aerosol concentrations and the contributions to haze events in China: an HTAP2 multi-model study

Haze has been severely affecting the densely populated areas in China recently. While many of the efforts have been devoted to investigating the impact of local anthropogenic emission, limited attention has been paid to the contribution from long-range transport. In this study, we apply simulations from six participating models supplied through the Task Force on Hemispheric Transport of Air Pollution phase 2 (HTAP2) exercise to investigate the long-range transport impact of Europe (EUR) and Russia–Belarus–Ukraine (RBU) on the surface air quality in eastern Asia(EAS), with special focus on their contributions during the haze episodes in China. The impact of 20 % anthropogenic emission perturbation from the source region is extrapolated by a factor of 5 to estimate the full impact.We find that the full impacts from EUR and RBU are 0.99 µg m -3 (3.1 %) and 1.32 µg m -3 (4.1 %) during haze episodes,while the annual averaged full impacts are only 0.35 µg m -3 (1.7 %) and 0.53 µg m -3 (2.6 %). By estimating the aerosol response within and above the planetary boundary layer (PBL), we find that long-range transport from EUR within the PBL contributes to 22–38 % of the total column density of aerosol response in EAS. Comparison with the HTAP phase 1 (HTAP1) assessment reveals that from 2000 to 2010, the long-range transport from Europe to eastern Asia has decreased significantly by a factor of 2–10 for surface aerosol mass concentration due to the simultaneous emission reduction in source regions and emission increase in the receptor region. We also find the long-range transport from the Europe and RBU regions increases the number of haze events in China by 0.15 % and 0.11 %, and the North China Plain and southeastern China has 1–3 extra haze days (<3 %). This study is the first investigation into the contribution of long-range transport to haze in China with multi-model experiments.

54 ENVIRONMENTAL SCIENCES↗

DOE OSTI2018

Holistic Assessment of SO 2 Injections Using CESM1(WACCM): Introduction to the Special Issue

We introduce a special issue on a holistic assessment of geoengineering via stratospheric SO 2 injection in the state-of-the-art climate model, Community Earth System Model, version 1 with the Whole Atmosphere Community Climate Model as its atmospheric component (CESM1(WACCM)). This model has numerous complexities that allow it to represent some of the most important nonlinearities associated with stratospheric SO 2 injection, including aerosol microphysical growth and stratospheric chemistry. The studies described herein represent the steps towards and first attempt in a state-of-the-art climate model to use geoengineering to meet multiple simultaneous objectives via SO 2 injection at multiple locations. First, a “matrix” of simulations was carried out to better understand the response of geoengineering to variations in latitude, altitude, and amount of sulfur dioxide injections. Subsequently, in a century long simulation, a feedback algorithm was employed to meet specific objectives and manage uncertainty, wherein the injection amount at each location was adjusted every model year. Most of the analyses contained in this special issue focus on surface climate and stratospheric changes in the matrix and century long simulations. In addition, 20 ensemble members of the feedback simulation have been carried out and provided to the community to expand the scope of analyses to low signal-to-noise ratio fields, including regional effects, impacts assessment, and extreme events. The demonstration provided by these simulations is a step toward understanding the space of achievable climate objectives via geoengineering, or, phrased differently, determining what geoengineering can do and what it cannot do.

54 ENVIRONMENTAL SCIENCES↗

DOE OSTI2018

Evaluating simplified chemical mechanisms within present-day simulations of the Community Earth System Model version 1.2 with CAM4 (CESM1.2 CAM-chem): MOZART-4 vs. Reduced Hydrocarbon vs. Super-Fast chemistry

Abstract. While state-of-the-art complex chemical mechanisms expand our understanding of atmospheric chemistry, their sheer size and computational requirements often limit simulations to short lengths or ensembles to only a few members. Here we present and compare three 25-year present-day offline simulations with chemical mechanisms of different levels of complexity using the Community Earth System Model (CESM) Version 1.2 CAM-chem (CAM4): the Model for Ozone and Related Chemical Tracers, version 4 (MOZART-4) mechanism, the Reduced Hydrocarbon mechanism, and the Super-Fast mechanism. We show that, for most regions and time periods, differences in simulated ozone chemistry between these three mechanisms are smaller than the model–observation differences themselves. The MOZART-4 mechanism and the Reduced Hydrocarbon are in close agreement in their representation of ozone throughout the troposphere during all time periods (annual, seasonal, and diurnal). While the Super-Fast mechanism tends to have higher simulated ozone variability and differs from the MOZART-4 mechanism over regions of high biogenic emissions, it is surprisingly capable of simulating ozone adequately given its simplicity. We explore the trade-offs between chemical mechanism complexity and computational cost by identifying regions where the simpler mechanisms are comparable to the MOZART-4 mechanism and regions where they are not. The Super-Fast mechanism is 3 times as fast as the MOZART-4 mechanism, which allows for longer simulations or ensembles with more members that may not be feasible with the MOZART-4 mechanism given limited computational resources.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

DOE OSTI2018

Maximizing ozone signals among chemical, meteorological, and climatological variability

The detection of meteorological, chemical, or other signals in modeled or observed air quality data – such as an estimate of a temporal trend in surface ozone data, or an estimate of the mean ozone of a particular region during a particular season – is a critical component of modern atmospheric chemistry. However, the magnitude of a surface air quality signal is generally small compared to the magnitude of the underlying chemical, meteorological, and climatological variabilities (and their interactions) that exist both in space and in time, and which include variability in emissions and surface processes. This can present difficulties for both policymakers and researchers as they attempt to identify the influence or signal of climate trends (e.g., any pauses in warming trends), the impact of enacted emission reductions policies (e.g., United States NO x State Implementation Plans), or an estimate of the mean state of highly variable data (e.g., summertime ozone over the northeastern United States). Here we examine the scale dependence of the variability of simulated and observed surface ozone data within the United States and the likelihood that a particular choice of temporal or spatial averaging scales produce a misleading estimate of a particular ozone signal. Our main objective is to develop strategies that reduce the likelihood of overconfidence in simulated ozone estimates. We find that while increasing the extent of both temporal and spatial averaging can enhance signal detection capabilities by reducing the noise from variability, a strategic combination of particular temporal and spatial averaging scales can maximize signal detection capabilities over much of the continental US. For signals that are large compared to the meteorological variability (e.g., strong emissions reductions), shorter averaging periods and smaller spatial averaging regions may be sufficient, but for many signals that are smaller than or comparable in magnitude to the underlying meteorological variability, we recommend temporal averaging of 10–15 years combined with some level of spatial averaging (up to several hundred kilometers). If this level of averaging is not practical (e.g., the signal being examined is at a local scale), we recommend some exploration of the spatial and temporal variability to provide context and confidence in the robustness of the result. These results are consistent between simulated and observed data, as well as within a single model with different sets of parameters. The strategies selected in this study are not limited to surface ozone data and could potentially maximize signal detection capabilities within a broad array of climate and chemical observations or model output.

54 ENVIRONMENTAL SCIENCES↗

NASA NTRS2018

Large-Scale Tropospheric Transport in the Chemistry-Climate Model Initiative (CCMI) Simulations

Understanding and modeling the large-scale transport of trace gases and aerosols is important for interpreting past (and projecting future) changes in atmospheric composition. Here we show that there are large differences in the global-scale atmospheric transport properties among the models participating in the IGAC SPARC Chemistry–Climate Model Initiative (CCMI). Specifically, we find up to 40% differences in the transport timescales connecting the Northern Hemisphere (NH) midlatitude surface to the Arctic and to Southern Hemisphere high latitudes, where the mean age ranges between 1.7 and 2.6 years. We show that these differences are related to large differences in vertical transport among the simulations, in particular to differences in parameterized convection over the oceans. While stronger convection over NH midlatitudes is associated with slower transport to the Arctic, stronger convection in the tropics and subtropics is associated with faster interhemispheric transport. We also show that the differences among simulations constrained with fields derived from the same reanalysis products are as large as (and in some cases larger than) the differences among free-running simulations, most likely due to larger differences in parameterized convection. Our results indicate that care must be taken when using simulations constrained with analyzed winds to interpret the influence of meteorology on tropospheric composition.

Orbe, Clara↗

DOE OSTI2018

Future heat waves and surface ozone

Not Available

54 ENVIRONMENTAL SCIENCES↗

NASA NTRS2018

Tropospheric Jet Response to Antarctic Ozone Depletion: An Update with Chemistry-Climate Model Initiative (CCMI) Models

The Southern Hemisphere (SH) zonal-mean circulation change in response to Antarctic ozone depletion is re-visited by examining a set of the latest model simulations archived for the Chemistry-Climate Model Initiative (CCMI) project. All models reasonably well reproduce Antarctic ozone depletion in the late 20th century. The related SH-summer circulation changes, such as a poleward intensification of westerly jet and a poleward expansion of the Hadley cell, are also well captured. All experiments exhibit quantitatively the same multi-model mean trend, irrespective of whether the ocean is coupled or prescribed. Results are also quantitatively similar to those derived from the Coupled Model Intercomparison Project phase 5 (CMIP5) high-top model simulations in which the stratospheric ozone is mostly prescribed with monthly- and zonally-averaged values. These results suggest that the ozone-hole-induced SH-summer circulation changes are robust across the models irrespective of the specific chemistry-atmosphere-ocean coupling.

chemistry-climate models↗

DOE OSTI2018

Impacts of Aerosol Dry Deposition on Black Carbon Spatial Distributions and Radiative Effects in the Community Atmosphere Model CAM5

Dry deposition is a vital process affecting the lifetime and spatial distributions of atmospheric aerosols. Black carbon (BC) plays an important role in the Earth’s climate. To explore the sensitivity of modeled BC spatial distributions to particle dry deposition treatments, the scheme of Petroff & Zhang (2010) (PZ10) is implemented into the Community Atmospheric Model version 5 (CAM5), and model simulations using PZ10 are compared with the one using the default scheme of Zhang et al. (2001) (Z01). The PZ10 scheme suggests much lower dry deposition velocities than Z01 for fine particles in Aitken, primary carbon, and accumulation modes, resulting in 73.0% lower of global mean BC dry deposition fluxes and 23.2% higher of global mean BC column burdens. CAM5 with PZ10 increases modeled BC concentrations at all altitudes and latitudes compared to Z01, which improves the agreement with observations of BC profiles in the lower troposphere in the Arctic. It also helps the simulation of surface BC concentrations in high-latitudes remote regions and its seasonality in the Arctic. Yet, PZ10 slightly exacerbates the overestimation of modeled BC concentrations in the middle and upper troposphere, which might be due to model uncertainties in other aerosol physical and chemical processes. The global annual mean radiative effects due to aerosol-radiation interactions (REari) and aerosol-cloud interactions (REaci) of BC from the CAM5 experiment using Z01 are 0.61±0.007 and -0.11±0.02 W m -2 , respectively, compared to slightly larger REari (0.75±0.01 W m -2 ) and REaci (-0.14±0.02 W m -2 ) from CAM5 using PZ10.

54 ENVIRONMENTAL SCIENCES↗

NASA NTRS2018

Multi-model Comparison of the Volcanic Sulfate Deposition from the 1815 Eruption of Mt. Tambora

The eruption of Mt. Tambora in 1815 was the largest volcanic eruption of the past 500 years. The eruption had significant climatic impacts, leading to the 1816 "year without a summer", and remains a valuable event from which to understand the climatic effects of large stratospheric volcanic sulfur dioxide injections. The eruption also resulted in one of the strongest and most easily identifiable volcanic sulfate signals in polar ice cores, which are widely used to reconstruct the timing and atmospheric sulfate loading of past eruptions. As part of the Model Intercomparison Project on the climatic response to Volcanic forcing (VolMIP), five state-of-the-art global aerosol models simulated this eruption. We analyze both simulated background (no Tambora) and volcanic (with Tambora) sulfate deposition to polar regions and compare to ice core records. The models simulate overall similar patterns of background sulfate deposition, although there are differences in regional details and magnitude. However, the volcanic sulfate deposition varies considerably between the models with differences in timing, spatial pattern and magnitude. Mean simulated deposited sulfate on Antarctica ranges from 19 to 264 kgkm-2 and on Greenland from 31 to 194 kgkm-2, as compared to the mean ice-core derived estimates of roughly 50 kgkm-2 for both Greenland and Antarctica. The ratio of the hemispheric atmospheric sulfate aerosol burden after the eruption to the average ice sheet deposited sulfate varies between models by up to a factor of 15. Sources of this inter-model variability include differences in both the formation and the transport of sulfate aerosol. Our results suggest that deriving relationships between sulfate deposited on ice sheets and atmospheric sulfate burdens from model simulations may be associated with greater uncertainties than previously thought.

Marshall, Lauren↗

DOE OSTI2017

The Climate Response to Stratospheric Aerosol Geoengineering Can Be Tailored Using Multiple Injection Locations

By injecting different amounts of SO 2 at multiple different latitudes, the spatial pattern of aerosol optical depth (AOD) can be partially controlled. This leads to the ability to influence the climate response to geoengineering with stratospheric aerosols, providing the potential for design. In this work, we use simulations from the fully coupled whole-atmosphere chemistry climate model CESM1(WACCM) to demonstrate that by appropriately combining injection at just four different locations, 30°S, 15°S, 15°N, and 30°N, then three spatial degrees of freedom of AOD can be achieved: an approximately spatially uniform AOD distribution, the relative difference in AOD between Northern and Southern Hemispheres, and the relative AOD in high versus low latitudes. For forcing levels that yield 1–2°C cooling, the AOD and surface temperature response are sufficiently linear in this model so that the response to different combinations of injection at different latitudes can be estimated from single-latitude injection simulations; nonlinearities associated with both aerosol growth and changes to stratospheric circulation will be increasingly important at higher forcing levels. Optimized injection at multiple locations is predicted to improve compensation of CO 2 -forced climate change relative to a case using only equatorial aerosol injection (which overcools the tropics relative to high latitudes). The additional degrees of freedom can be used, for example, to balance the interhemispheric temperature gradient and the equator to pole temperature gradient in addition to the global mean temperature. Further research is needed to better quantify the impacts of these strategies on changes to long-term temperature, precipitation, and other climate parameters.

54 ENVIRONMENTAL SCIENCES↗

DOE OSTI2017

First Simulations of Designing Stratospheric Sulfate Aerosol Geoengineering to Meet Multiple Simultaneous Climate Objectives

In this work, we describe the first simulations of stratospheric sulfate aerosol geoengineering using multiple injection locations to meet multiple simultaneous surface temperature objectives. Simulations were performed using CESM1(WACCM), a coupled atmosphere-ocean general circulation model with fully interactive stratospheric chemistry, dynamics (including an internally generated quasi-biennial oscillation), and a sophisticated treatment of sulfate aerosol formation, microphysical growth, and deposition. The objectives are defined as maintaining three temperature features at their 2020 levels against a background of the RCP8.5 scenario over the period 2020-2099. These objectives are met using a feedback mechanism in which the rate of sulfur dioxide injection at each of the four locations is adjusted independently every year of simulation. Even in the presence of uncertainties, nonlinearities, and variability, the objectives are met, predominantly by SO2 injection at 30°N and 30°S. By the last year of simulation, the feedback algorithm calls for a total injection rate of 51 Tg SO2 per year. The injections are not in the tropics, which results in a greater degree of linearity of the surface climate response with injection amount than has been found in many previous studies using injection at the equator. Because the objectives are defined in terms of annual mean temperature, the required geeongineering results in "overcooling" during summer and "undercooling" during winter. The hydrological cycle is also suppressed as compared to the reference values corresponding to the year 2020. The demonstration we describe in this study is an important step toward understanding what geoengineering can do and what it cannot do.

54 ENVIRONMENTAL SCIENCES↗