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Excess deposition (including both wet and dry deposition) of nitrogen and sulfur is detrimental to ecosystems. Recent studies have investigated the spatial patterns and temporal trends of nitrogen and sulfur wet deposition, but few studies have focused on dry deposition due to the scarcity of dry deposition measurements. Here, we use long-term model simulations from the coupled Weather Research and Forecasting and the Community Multiscale Air Quality (WRF-CMAQ) model covering the period from 1990 to 2010 to study changes in spatial distribution as well as temporal trends in total (TDEP), wet (WDEP), and dry deposition (DDEP) of total inorganic nitrogen (TIN) and sulfur (TS) in the United States (US). We first evaluate the model's performance in simulating WDEP over the US by comparing the model results with observational data from the US National Atmospheric Deposition Program. The coupled model generally underestimates the WDEP of both TIN (including both the oxidized nitrogen deposition, TNO3, and the reduced nitrogen deposition, NHx) and TS, with better performance in the eastern US than the western US. The underestimation of the wet deposition by the model is mainly caused by the coarse model grid resolution, missing lightning NOx emissions, and the poor temporal and spatial representation of NH3 emissions. TDEP of both TIN and TS shows significant decreases over the US, especially in the east, due to the large emission reductions that occurred in that region. The decreasing trends of TIN TDEP are caused by decreases in TNO3, and the increasing trends of TIN deposition over the Great Plains and Tropical Wet Forests (Southern Florida Coastal Plain) regions are caused by increases in NH3 emissions, although it should be noted that these increasing trends are not significant. TIN WDEP shows decreasing trends throughout the US, except for the Marine West Coast Forest region. TIN DDEP shows significant decreasing trends in the Eastern Temperate Forests, Northern Forests, Mediterranean California, and Marine West Coast Forest and significant increasing trends in the Tropical Wet Forests, Great Plains and Southern Semi-arid Highlands. For the other three regions (North American Deserts, Temperate Sierras, and Northwestern Forested Mountains), the decreasing or increasing trends are not significant. Both the WDEP and DDEP of TS have decreases across the US, with a larger decreasing trend in the DDEP than that in the WDEP. Across the US during the 1990–2010 period, DDEP of TIN accounts for 58–65 % of TDEP of TIN. TDEP of TIN over the US is dominated by deposition of TNO3 during the first decade, which then shifts to reduced nitrogen (NHx) dominance after 2003, resulting from a combination of NOx emission reductions and NH3 emission increases. The sulfur DDEP is usually higher than the sulfur WDEP until recent years, as the sulfur DDEP has a larger decreasing trend than WDEP.

Concentrations of both fine particulate matter (PM2.5) and ozone (O3) in the United States (US) have decreased significantly since 1990, mainly because of air quality regulations. Exposure to these air pollutants is associated with premature death. Here we quantify the annual mortality burdens from PM2.5 and O3 in the US from 1990 to 2010, estimate trends and inter-annual variability, and evaluate the contributions to those trends from changes in pollutant concentrations, population, and baseline mortality rates. We use a fine-resolution (36 km) self-consistent 21-year simulation of air pollutant concentrations in the US from 1990 to 2010, a health impact function, and annual county-level population and baseline mortality rate estimates. From 1990 to 2010, the modeled population-weighted annual PM2.5 decreased by 39 %, and summertime (April to September) 1 h average daily maximum O3 decreased by 9 % from 1990 to 2010. The PM2.5-related mortality burden from ischemic heart disease, chronic obstructive pulmonary disease, lung cancer, and stroke steadily decreased by 54 % from 123 700 deaths year−1 (95 % confidence interval, 70 800–178 100) in 1990 to 58 600 deaths year−1 (24 900–98 500) in 2010. The PM2.5-related mortality burden would have decreased by only 24 % from 1990 to 2010 if the PM2.5 concentrations had stayed at the 1990 level, due to decreases in baseline mortality rates for major diseases affected by PM2.5. The mortality burden associated with O3 from chronic respiratory disease increased by 13 % from 10 900 deaths year−1 (3700–17 500) in 1990 to 12 300 deaths year−1 (4100–19 800) in 2010, mainly caused by increases in the baseline mortality rates and population, despite decreases in O3 concentration. The O3-related mortality burden would have increased by 55 % from 1990 to 2010 if the O3 concentrations had stayed at the 1990 level. The detrended annual O3 mortality burden has larger inter-annual variability (coefficient of variation of 12 %) than the PM2.5-related burden (4 %), mainly from the inter-annual variation of O3 concentration. We conclude that air quality improvements have significantly decreased the mortality burden, avoiding roughly 35 800 (38 %) PM2.5-related deaths and 4600 (27 %) O3-related deaths in 2010, compared to the case if air quality had stayed at 1990 levels (at 2010 baseline mortality rates and population).

Regional, state, and local environmental regulatory agencies often use Eulerian models to investigate the potential impacts on pollutant deposition and air quality from changes in land use, anthropogenic and natural emissions, and climate. The Noah land surface model (LSM) in the Weather Research and Forecasting (WRF) model is widely used with the Community Multiscale Air Quality (CMAQ) model for such investigations, but there are many inconsistencies that need to be changed so that they are consistent with dry deposition and emission processes. In this work, the Noah LSM in WRFv3.8.1 is improved in its linkage to CMAQv5.2 by adding important parameters to the WRF/Noah output, updating the WRF soil and vegetation reference tables that influence CMAQ wet and dry photochemical deposition processes, and decreasing WRF/Noah's top soil layer depth to be consistent with CMAQ processes (e.g., windblown dust and bidirectional ammonia exchange). The modified WRF/Noah‐CMAQ system (both off‐line and coupled) impacts meteorological predictions of 2‐m temperature (T2; increases and decreases), 2‐m mixing ratio (Q2; decreases), and 10‐m wind speed (WSPD10; decreases) in the United States. These changes are mostly driven by leaf area index values and aerodynamic roughness lengths updated in the vegetation tables based on satellite data, with additional impacts from soil tables updated based on recent soil data. Improvements in the consistency in the treatment of land surface processes between CMAQ and WRF resulted in improvements in both estimated meteorological (e.g., T2, WSPD10, and latent heat fluxes) and chemical (e.g., ozone, sulfur dioxide, and windblown dust) model estimates. Plain Language Summary In this study we update a robust and well‐established coupled meteorology‐chemistry model, via the use of advanced treatments of land‐atmosphere characteristics and processes, as well as improved linkages for a commonly used land surface model in weather, climate, and air quality applications. The updated model shows improved predictions of important weather and air quality parameters, such as temperature, wind speed, and ozone when compared to observations in the United States. Overall, the updated modeling system more firmly establishes the physical connections between the land and atmosphere to expand the model to a wider array of weather, climate, and air quality applications. Key Points The Noah land surface model is updated for its linkage and consistency in a meteorological‐air quality modeling system The advanced land‐atmosphere characteristics and processes allow for a more accurate and usable coupled air quality modeling system The updated air quality model shows improved meteorological and air quality predictions compared to observations in the United States

We present the collective evaluation of the regional-scale models that took part in the fourth edition of the Air Quality Model Evaluation International Initiative (AQMEII). The activity consists of the evaluation and intercomparison of regional-scale air quality models run over North American (NA) and European (EU) domains for 2016 (NA) and 2010 (EU). The focus of the paper is ozone dry deposition. Dry deposition is among the most important processes of removal of chemical compounds from the atmosphere and an important contributor to the overall chemical budget of the latter. Furthermore ozone dry deposition is very important as it can be severely detrimental to vegetation physiology. The collective evaluation begins with an operational evaluation, namely a direct comparison of model-simulated predictions with monitoring data aiming at assessing model performance (Dennis et al., 2010). Following the AQMEII protocol and Dennis et al. (2010), we also perform a probabilistic evaluation in the form of ensemble analyses and an introductory diagnostic evaluation. The latter analyzes the role of dry deposition in comparison with dynamic and radiative processes and land use/land cover (LULC) types in determining surface ozone variability. Important differences are found across dry deposition results when the same LULC is considered. Furthermore, we found that models use very different LULC masks, thus introducing an additional level of diversity in the model results. The study stresses that, as for other kinds of prior and problem-defining information (emissions, topography, or land–water masks), the choice of LULC mask should not be at modeler discretion. Furthermore, LULC should be considered as a variable to be evaluated in any future model intercomparison, unless set as common input information. The differences in LULC selection can have a substantial impact on model results, making the task of evaluating dry deposition modules across different regional-scale models very difficult.

Atmospheric deposition of nitrogen (N) and sulfur (S) compounds from human activity has greatly declined in the United States (US) over the past several decades in response to emission controls set by the Clean Air Act. While many observational studies have investigated spatial and temporal trends of atmospheric deposition, modeling assessments can provide useful information over areas with sparse measurements, although they usually have larger horizontal resolutions and are limited by input data availability. In this analysis, we evaluate wet, dry, and total N and S deposition from multiyear simulations within the contiguous US (CONUS). Community Multiscale Air Quality (CMAQ) model estimates from the EPA's (Environmental Protection Agency) Air QUAlity TimE Series (EQUATES) project contain important model updates to atmospheric deposition algorithms compared to previous model data, including the new Surface Tiled Aerosol and Gaseous Exchange (STAGE) bidirectional deposition model which contains land-use-specific resistance parameterization and land-use-specific deposition estimates needed to estimate the differential impacts of N deposition to different land use types. First, we evaluate model estimates of wet deposition and ambient concentrations, finding underestimates of SO4, NO3, and NH4 wet deposition compared to National Atmospheric Deposition Program observations and underestimates of NH4 and SO4 and overestimates of SO2 and TNO3 (HNO3+NO3) compared to the Clean Air Status and Trends Network (CASTNET) ambient concentrations. Second, a measurement–model fusion approach employing a precipitation and bias correction to wet-deposition estimates is found to reduce model bias and improve correlations compared to the unadjusted model values. Model agreement of wet deposition is poor over parts of the West and Northern Rockies, due to errors in precipitation estimates caused by complex terrain and uncertainty in emissions at the relatively coarse 12 km grid resolution used in this study. Next, we assess modeled N and S deposition trends across climatologically consistent regions in the CONUS. Total deposition of N and S in the eastern US is larger than the western US with a steeper decreasing trend from 2002–2017; i.e., total N declined at a rate of approximately −0.30 kg N ha−1 yr−1 in the Northeast and Southeast and by −0.02 kg N ha−1 yr−1 in the Northwest and Southwest. Widespread increases in reduced N deposition across the Upper Midwest, Northern Rockies, and West indicate evolving atmospheric composition due to increased precipitation amounts over some areas, growing agricultural emissions, and regional NOx/SOx emission reductions shifting gas–aerosol partitioning; these increases in reduced N deposition are generally masked by the larger decreasing oxidized N trend. We find larger average declining trends of total N and S deposition between 2002–2009 than 2010–2017, suggesting a slowdown of the rate of decline likely in response to smaller emission reductions. Finally, we document changes in the modeled total N and S deposition budgets. The average annual total N deposition budget over the CONUS decreases from 7.8 in 2002 to 6.3 kg N ha−1 yr−1 in 2017 due to declines in oxidized N deposition from NOx emission controls. Across the CONUS during the 2002–2017 time period, the average contribution of dry deposition to the total N deposition budget drops from 60 % to 52 %, whereas wet deposition dominates the S budget rising from 45 % to 68 %. Our analysis extends upon the literature documenting the growing contribution of reduced N to the total deposition budget, particularly in the Upper Midwest and Northern Rockies, and documents a slowdown of the declining oxidized N deposition trend, which may have consequences on vegetation diversity and productivity.

The Community Multiscale Air Quality (CMAQ) model version 5.3 (CMAQ53), released to the public in August 2019 and followed by version 5.3.1 (CMAQ531) in December 2019, contains numerous science updates, enhanced functionality, and improved computation efficiency relative to the previous version of the model, 5.2.1 (CMAQ521). Major science advances in the new model include a new aerosol module (AERO7) with significant updates to secondary organic aerosol (SOA) chemistry, updated chlorine chemistry, updated detailed bromine and iodine chemistry, updated simple halogen chemistry, the addition of dimethyl sulfide (DMS) chemistry in the CB6r3 chemical mechanism, updated M3Dry bidirectional deposition model, and the new Surface Tiled Aerosol and Gaseous Exchange (STAGE) bidirectional deposition model. In addition, support for the Weather Research and Forecasting (WRF) model's hybrid vertical coordinate (HVC) was added to CMAQ53 and the Meteorology-Chemistry Interface Processor (MCIP) version 5.0 (MCIP50). Enhanced functionality in CMAQ53 includes the new Detailed Emissions Scaling, Isolation and Diagnostic (DESID) system for scaling incoming emissions to CMAQ and reading multiple gridded input emission files.Evaluation of CMAQ531 was performed by comparing monthly and seasonal mean daily 8 h average (MDA8) O3 and daily PM2.5 values from several CMAQ531 simulations to a similarly configured CMAQ521 simulation encompassing 2016. For MDA8 O3, CMAQ531 has higher O3 in the winter versus CMAQ521, due primarily to reduced dry deposition to snow, which strongly reduces wintertime O3 bias (2–4 ppbv monthly average). MDA8 O3 is lower with CMAQ531 throughout the rest of the year, particularly in spring, due in part to reduced O3 from the lateral boundary conditions (BCs), which generally increases MDA8 O3 bias in spring and fall (∼0.5 µgm-3). For daily 24 h average PM2.5, CMAQ531 has lower concentrations on average in spring and fall, higher concentrations in summer, and similar concentrations in winter to CMAQ521, which slightly increases bias in spring and fall and reduces bias in summer. Comparisons were also performed to isolate updates to several specific aspects of the modeling system, namely the lateral BCs, meteorology model version, and the deposition model used. Transitioning from a hemispheric CMAQ (HCMAQ) version 5.2.1 simulation to a HCMAQ version 5.3 simulation to provide lateral BCs contributes to higher O3 mixing ratios in the regional CMAQ simulation in higher latitudes during winter (due to the decreased O3 dry deposition to snow in CMAQ53) and lower O3 mixing ratios in middle and lower latitudes year-round (due to reduced O3 over the ocean with CMAQ53). Transitioning from WRF version 3.8 to WRF version 4.1.1 with the HVC resulted in consistently higher (1.0–1.5 ppbv) MDA8 O3 mixing ratios and higher PM2.5 concentrations (0.1–0.25 µgm-3) throughout the year. Finally, comparisons of the M3Dry and STAGE deposition models showed that MDA8 O3 is generally higher with M3Dry outside of summer, while PM2.5 is consistently higher with STAGE due to differences in the assumptions of particle deposition velocities to non-vegetated surfaces and land use with short vegetation (e.g., grasslands) between the two models. For ambient NH3, STAGE has slightly higher concentrations and smaller bias in the winter, spring, and fall, while M3Dry has higher concentrations and smaller bias but larger error and lower correlation in the summer.

Recent studies have shown that exposure to particulate black carbon (BC) has significant adverse health effects and may be more detrimental to human health than exposure to PM2.5 as a whole. Mobile source BC emission controls, mostly on diesel-burning vehicles, have successfully decreased mobile source BC emissions to less than half of what they were 30 years ago. Quantification of the benefits of previous emissions controls conveys the value of these regulatory actions and provides a method by which future control alternatives could be evaluated. In this study we use the adjoint of the Community Multiscale Air Quality (CMAQ) model to estimate highly-resolved spatial distributions of benefits related to emission reductions for six urban regions within the continental US. Emissions from outside each of the six chosen regions account for between 7% and 27% of the premature deaths attributed to exposure to BC within the region. While we estimate that nonroad mobile and onroad diesel emissions account for the largest number of premature deaths attributable to exposure to BC, onroad gasoline is shown to have more than double the benefit per unit emission relative to that of nonroad mobile and onroad diesel. Within the region encompassing New York City and Philadelphia, reductions in emissions from large industrial combustion sources that are not classified as EGUs (i.e., non-EGU) are estimated to have up to triple the benefits per unit emission relative to reductions to onroad diesel sectors, and provide similar benefits per unit emission to that of onroad gasoline emissions in the region. While onroad mobile emissions have been decreasing in the past 30 years and a majority of vehicle emission controls that regulate PM focus on diesel emissions, our analysis shows the most efficient target for stricter controls is actually onroad gasoline emissions.

Existing descriptions of bi-directional ammonia (NH3) land–atmosphere exchange incorporate temperature and moisture controls, and are beginning to be used in regional chemical transport models. However, such models have typically applied simpler emission factors to upscale the main NH3 emission terms. While this approach has successfully simulated the main spatial patterns on local to global scales, it fails to address the environment- and climate-dependence of emissions. To handle these issues, we outline the basis for a new modelling paradigm where both NH3 emissions and deposition are calculated online according to diurnal, seasonal and spatial differences in meteorology. We show how measurements reveal a strong, but complex pattern of climatic dependence, which is increasingly being characterized using ground-based NH3 monitoring and satellite observations, while advances in process-based modelling are illustrated for agricultural and natural sources, including a global application for seabird colonies. A future architecture for NH3 emission–deposition modelling is proposed that integrates the spatio-temporal interactions, and provides the necessary foundation to assess the consequences of climate change. Based on available measurements, a first empirical estimate suggests that 5°C warming would increase emissions by 42 per cent (28–67%). Together with increased anthropogenic activity, global NH3 emissions may increase from 65 (45–85) Tg N in 2008 to reach 132 (89–179) Tg by 2100.

The Community Multiscale Air Quality (CMAQ) model is a comprehensive multipollutant air quality modeling system developed and maintained by the US Environmental Protection Agency's (EPA) Office of Research and Development (ORD). Recently, version 5.1 of the CMAQ model (v5.1) was released to the public, incorporating a large number of science updates and extended capabilities over the previous release version of the model (v5.0.2). These updates include the following: improvements in the meteorological calculations in both CMAQ and the Weather Research and Forecast (WRF) model used to provide meteorological fields to CMAQ, updates to the gas and aerosol chemistry, revisions to the calculations of clouds and photolysis, and improvements to the dry and wet deposition in the model. Sensitivity simulations isolating several of the major updates to the modeling system show that changes to the meteorological calculations result in enhanced afternoon and early evening mixing in the model, periods when the model historically underestimates mixing. This enhanced mixing results in higher ozone (O3) mixing ratios on average due to reduced NO titration, and lower fine particulate matter (PM2. 5) concentrations due to greater dilution of primary pollutants (e.g., elemental and organic carbon). Updates to the clouds and photolysis calculations greatly improve consistency between the WRF and CMAQ models and result in generally higher O3 mixing ratios, primarily due to reduced cloudiness and attenuation of photolysis in the model. Updates to the aerosol chemistry result in higher secondary organic aerosol (SOA) concentrations in the summer, thereby reducing summertime PM2. 5 bias (PM2. 5 is typically underestimated by CMAQ in the summer), while updates to the gas chemistry result in slightly higher O3 and PM2. 5 on average in January and July. Overall, the seasonal variation in simulated PM2. 5 generally improves in CMAQv5.1 (when considering all model updates), as simulated PM2. 5 concentrations decrease in the winter (when PM2. 5 is generally overestimated by CMAQ) and increase in the summer (when PM2. 5 is generally underestimated by CMAQ). Ozone mixing ratios are higher on average with v5.1 vs. v5.0.2, resulting in higher O3 mean bias, as O3 tends to be overestimated by CMAQ throughout most of the year (especially at locations where the observed O3 is low); however, O3 correlation is largely improved with v5.1. Sensitivity simulations for several hypothetical emission reduction scenarios show that v5.1 tends to be slightly more responsive to reductions in NOx (NO + NO2), VOC and SOx (SO2 + SO4) emissions than v5.0.2, representing an improvement as previous studies have shown CMAQ to underestimate the observed reduction in O3 due to large, widespread reductions in observed emissions.

Biogenic volatile organic compounds (BVOC) participate in reactions that can lead to secondarily formed ozone and particulate matter (PM) impacting air quality and climate. BVOC emissions are important inputs to chemical transport models applied on local to global scales but considerable uncertainty remains in the representation of canopy parameterizations and emission algorithms from different vegetation species. The Biogenic Emission Inventory System (BEIS) has been used to support both scientific and regulatory model assessments for ozone and PM. Here we describe a new version of BEIS which includes updated input vegetation data and canopy model formulation for estimating leaf temperature and vegetation data on estimated BVOC. The Biogenic Emission Landuse Database (BELD) was revised to incorporate land use data from the Moderate Resolution Imaging Spectroradiometer (MODIS) land product and 2006 National Land Cover Database (NLCD) land coverage. Vegetation species data are based on the US Forest Service (USFS) Forest Inventory and Analysis (FIA) version 5.1 for 2002–2013 and US Department of Agriculture (USDA) 2007 census of agriculture data. This update results in generally higher BVOC emissions throughout California compared with the previous version of BEIS. Baseline and updated BVOC emission estimates are used in Community Multiscale Air Quality (CMAQ) Model simulations with 4 km grid resolution and evaluated with measurements of isoprene and monoterpenes taken during multiple field campaigns in northern California. The updated canopy model coupled with improved land use and vegetation representation resulted in better agreement between CMAQ isoprene and monoterpene estimates compared with these observations.