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Featured researches published by Barron H. Henderson.


Science of The Total Environment | 2016

A land use regression application into assessing spatial variation of intra-urban fine particulate matter (PM2.5) and nitrogen dioxide (NO2) concentrations in City of Shanghai, China

Chao Liu; Barron H. Henderson; Dongfang Wang; Xinyuan Yang; Zhong-Ren Peng

Intra-urban assessment of air pollution exposure has become a priority study while international attention was attracted to PM2.5 pollution in China in recent years. Land Use Regression (LUR), which has previously been proved to be a feasible way to describe the relationship between land use and air pollution level in European and American cities, was employed in this paper to explain the correlations and spatial variations in Shanghai, China. PM2.5 and NO2 concentrations at 35-45 monitoring locations were selected as dependent variables, and a total of 44 built environmental factors were extracted as independent variables. Only five factors showed significant explanatory value for both PM2.5 and NO2 models: longitude, distance from monitors to the ocean, highway intensity, waterbody area, and industrial land area for PM2.5 model; residential area, distance to the coast, industrial area, urban district, and highway intensity for NO2 model. Respectively, both PM2.5 and NO2 showed anti-correlation with coastal proximity (an indicator of clean air dilution) and correlation with highway and industrial intensity (source indicators). NO2 also showed significant correlation with local indicators of population density (residential intensity and urban classification), while PM2.5 showed significant correlation with regional dilution (longitude as a indicator of distance from polluted neighbors and local water features). Both adjusted R squared values were strong with PM2.5 (0.88) being higher than NO2 (0.62). The LUR was then used to produce continuous concentration fields for NO2 and PM2.5 to illustrate the features and, potentially, for use by future studies. Comparison to PM2.5 studies in New York and Beijing show that Shanghai PM2.5 pollutant distribution was more sensitive to geographic location and proximity to neighboring regions.


Science of The Total Environment | 2016

Assessing public health burden associated with exposure to ambient black carbon in the United States.

Ying Li; Daven K. Henze; Darby Jack; Barron H. Henderson; Patrick L. Kinney

Black carbon (BC) is a significant component of fine particulate matter (PM2.5) air pollution, which has been linked to a series of adverse health effects, in particular premature mortality. Recent scientific research indicates that BC also plays an important role in climate change. Therefore, controlling black carbon emissions provides an opportunity for a double dividend. This study quantifies the national burden of mortality and morbidity attributable to exposure to ambient BC in the United States (US). We use GEOS-Chem, a global 3-D model of atmospheric composition to estimate the 2010 annual average BC levels at 0.5×0.667° resolution, and then re-grid to 12-km grid resolution across the continental US. Using PM2.5 mortality risk coefficient drawn from the American Cancer Society cohort study, the numbers of deaths due to BC exposure were estimated for each 12-km grid, and then aggregated to the county, state and national level. Given evidence that BC particles may pose a greater risk on human health than other components of PM2.5, we also conducted sensitivity analysis using BC-specific risk coefficients drawn from recent literature. We estimated approximately 14,000 deaths to result from the 2010 BC levels, and hundreds of thousands of illness cases, ranging from hospitalizations and emergency department visits to minor respiratory symptoms. Sensitivity analysis indicates that the total BC-related mortality could be even significantly larger than the above mortality estimate. Our findings indicate that controlling BC emissions would have substantial benefits for public health in the US.


Journal of The Air & Waste Management Association | 2010

The influence of model resolution on ozone in industrial volatile organic compound plumes

Barron H. Henderson; Harvey E. Jeffries; Byeong-Uk Kim; William Vizuete

Abstract Regions with concentrated petrochemical industrial activity (e.g., Houston or Baton Rouge) frequently experience large, localized releases of volatile organic compounds (VOCs). Aircraft measurements suggest these released VOCs create plumes with ozone (O3) production rates 2–5 times higher than typical urban conditions. Modeling studies found that simulating high O3 productions requires superfine (1-km) horizontal grid cell size. Compared with fine modeling (4-km), the superfine resolution increases the peak O3 concentration by as much as 46%. To understand this drastic O3 change, this study quantifies model processes for O3 and “odd oxygen” (Ox) in both resolutions. For the entire plume, the superfine resolution increases the maximum O3 concentration 3% but only decreases the maximum Ox concentration 0.2%. The two grid sizes produce approximately equal Ox mass but by different reaction pathways. Derived sensitivity to oxides of nitrogen (NOx) and VOC emissions suggests resolution-specific sensitivity to NOx and VOC emissions. Different sensitivity to emissions will result in different O3 responses to subsequently encountered emissions (within the city or downwind). Sensitivity of O3 to emission changes also results in different simulated O3 responses to the same control strategies. Sensitivity of O3 to NOx and VOC emission changes is attributed to finer resolved Eulerian grid and finer resolved NOx emissions. Urban NOx concentration gradients are often caused by roadway mobile sources that would not typically be addressed with Plume-in-Grid models. This study shows that grid cell size (an artifact of modeling) influences simulated control strategies and could bias regulatory decisions. Understanding the dynamics of VOC plume dependence on grid size is the first step toward providing more detailed guidance for resolution. These results underscore VOC and NOx resolution interdependencies best addressed by finer resolution. On the basis of these results, the authors suggest a need for quantitative metrics for horizontal grid resolution in future model guidance.


Journal of Geophysical Research | 2016

Observational constraints on glyoxal production from isoprene oxidation and its contribution to organic aerosol over the Southeast United States

Jingyi Li; Jingqiu Mao; Kyung-Eun Min; Rebecca A. Washenfelder; Steven S. Brown; Jennifer Kaiser; Frank N. Keutsch; R. Volkamer; Glenn M. Wolfe; T. F. Hanisco; Ilana B. Pollack; Thomas B. Ryerson; Martin Graus; J. B. Gilman; Carsten Warneke; Joost A. de Gouw; Ann M. Middlebrook; Jin Liao; André Welti; Barron H. Henderson; V. Faye McNeill; Samuel R. Hall; Kirk Ullmann; Leo J. Donner; Fabien Paulot; Larry W. Horowitz

We use a 0-D photochemical box model and a 3-D global chemistry-climate model, combined with observations from the NOAA Southeast Nexus (SENEX) aircraft campaign, to understand the sources and sinks of glyoxal over the Southeast United States. Box model simulations suggest a large difference in glyoxal production among three isoprene oxidation mechanisms (AM3ST, AM3B, and MCM v3.3.1). These mechanisms are then implemented into a 3-D global chemistry-climate model. Comparison with field observations shows that the average vertical profile of glyoxal is best reproduced by AM3ST with an effective reactive uptake coefficient γglyx of 2 × 10-3, and AM3B without heterogeneous loss of glyoxal. The two mechanisms lead to 0-0.8 μg m-3 secondary organic aerosol (SOA) from glyoxal in the boundary layer of the Southeast U.S. in summer. We consider this to be the lower limit for the contribution of glyoxal to SOA, as other sources of glyoxal other than isoprene are not included in our model. In addition, we find that AM3B shows better agreement on both formaldehyde and the correlation between glyoxal and formaldehyde (RGF = [GLYX]/[HCHO]), resulting from the suppression of δ-isoprene peroxy radicals (δ-ISOPO2). We also find that MCM v3.3.1 may underestimate glyoxal production from isoprene oxidation, in part due to an underestimated yield from the reaction of IEPOX peroxy radicals (IEPOXOO) with HO2. Our work highlights that the gas-phase production of glyoxal represents a large uncertainty in quantifying its contribution to SOA.


Journal of Applied Meteorology and Climatology | 2017

Comparing Standard to Feature-Based Meteorological Model Evaluation Techniques in Bogotá, Colombia

Robert Nedbor-Gross; Barron H. Henderson; Justin R. Davis; Jorge E. Pachon; Alexander Rincón; Oscar J. Guerrero; Freddy Grajales

AbstractStandard meteorological model performance evaluation (sMPE) can be insufficient in determining “fitness” for air quality modeling. An sMPE compares predictions of meteorological variables with community-based thresholds. Conceptually, these thresholds measure the model’s capability to represent mesoscale features that cause variability in air pollution. A method that instead examines features could provide a better estimate of fitness. This work compares measures of fitness from sMPE analysis with a feature-based MPE (fMPE). Meteorological simulations for Bogota, Colombia, using the Weather Research and Forecasting (WRF) Model provide an ideal case study that highlights the importance of fMPE. Bogota is particularly interesting because the complex topography presents challenges for WRF in sMPE. A cluster analysis identified four dominant meteorological features associated with air quality driven by wind patterns. The model predictions are able to pass several sMPE thresholds but show poor performa...


Atmospheric Chemistry and Physics | 2011

Impact of lightning-NO on eastern United States photochemistry during the summer of 2006 as determined using the CMAQ model

Dale J. Allen; Kenneth E. Pickering; Robert W. Pinder; Barron H. Henderson; K. W. Appel; A. Prados


Geoscientific Model Development | 2013

A database and tool for boundary conditions for regional air quality modeling: description and evaluation

Barron H. Henderson; F. Akhtar; Havala O. T. Pye; Sergey L. Napelenok; William T. Hutzell


Atmospheric Environment | 2008

Modeling ozone formation from industrial emission events in Houston, Texas

William Vizuete; Byeong-Uk Kim; Harvey E. Jeffries; Yosuke Kimura; David T. Allen; Marianthi Anna Kioumourtzoglou; Leiran Biton; Barron H. Henderson


Atmospheric Chemistry and Physics | 2013

A comparison of atmospheric composition using the Carbon Bond and Regional Atmospheric Chemistry Mechanisms

Golam Sarwar; James M. Godowitch; Barron H. Henderson; Kathleen M. Fahey; George Pouliot; William T. Hutzell; Rohit Mathur; Daiwen Kang; Wendy S. Goliff; William R. Stockwell


Atmospheric Chemistry and Physics | 2013

Slower ozone production in Houston, Texas following emission reductions: evidence from Texas Air Quality Studies in 2000 and 2006

W. Zhou; Daniel S. Cohan; Barron H. Henderson

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William Vizuete

University of North Carolina at Chapel Hill

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Harvey E. Jeffries

University of North Carolina at Chapel Hill

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Giulia Ruggeri

École Polytechnique Fédérale de Lausanne

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Satoshi Takahama

École Polytechnique Fédérale de Lausanne

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Byeong-Uk Kim

University of North Carolina at Chapel Hill

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Carsten Warneke

Cooperative Institute for Research in Environmental Sciences

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David T. Allen

University of Texas at Austin

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