10-year spatial and temporal trends of PM<sub>2.5</sub> concentrations in the southeastern US estimated using high-resolution satellite data

Long-term PM<sub>2.5</sub> exposure has been associated with various adverse health outcomes. However, most ground monitors are located in urban areas, leading to a potentially biased representation of true regional PM<sub>2.5</sub> levels. To facilitate epidemiological studi...

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Main Authors: X. Hu, L. A. Waller, A. Lyapustin, Y. Wang, Y. Liu
Format: Article
Language:English
Published: Copernicus Publications 2014-06-01
Series:Atmospheric Chemistry and Physics
Online Access:http://www.atmos-chem-phys.net/14/6301/2014/acp-14-6301-2014.pdf
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spelling doaj-7b8f446daec849dcafe61b6b5cd094352020-11-25T01:02:09ZengCopernicus PublicationsAtmospheric Chemistry and Physics1680-73161680-73242014-06-0114126301631410.5194/acp-14-6301-201410-year spatial and temporal trends of PM<sub>2.5</sub> concentrations in the southeastern US estimated using high-resolution satellite dataX. Hu0L. A. Waller1A. Lyapustin2Y. Wang3Y. Liu4Department of Environmental Health, Rollins School of Public Health, Emory University, Atlanta, GA 30322, USADepartment of Biostatistics & Bioinformatics, Rollins School of Public Health, Emory University, Atlanta, GA 30322, USANASA Goddard Space Flight Center, Greenbelt, MD, USANASA Goddard Space Flight Center, Greenbelt, MD, USADepartment of Environmental Health, Rollins School of Public Health, Emory University, Atlanta, GA 30322, USALong-term PM<sub>2.5</sub> exposure has been associated with various adverse health outcomes. However, most ground monitors are located in urban areas, leading to a potentially biased representation of true regional PM<sub>2.5</sub> levels. To facilitate epidemiological studies, accurate estimates of the spatiotemporally continuous distribution of PM<sub>2.5</sub> concentrations are important. Satellite-retrieved aerosol optical depth (AOD) has been increasingly used for PM<sub>2.5</sub> concentration estimation due to its comprehensive spatial coverage. Nevertheless, previous studies indicated that an inherent disadvantage of many AOD products is their coarse spatial resolution. For instance, the available spatial resolutions of the Moderate Resolution Imaging Spectroradiometer (MODIS) and the Multiangle Imaging SpectroRadiometer (MISR) AOD products are 10 and 17.6 km, respectively. In this paper, a new AOD product with 1 km spatial resolution retrieved by the multi-angle implementation of atmospheric correction (MAIAC) algorithm based on MODIS measurements was used. A two-stage model was developed to account for both spatial and temporal variability in the PM<sub>2.5</sub>–AOD relationship by incorporating the MAIAC AOD, meteorological fields, and land use variables as predictors. Our study area is in the southeastern US centered at the Atlanta metro area, and data from 2001 to 2010 were collected from various sources. The model was fitted annually, and we obtained model fitting <i>R</i><sup>2</sup> ranging from 0.71 to 0.85, mean prediction error (MPE) from 1.73 to 2.50 μg m<sup>−3</sup>, and root mean squared prediction error (RMSPE) from 2.75 to 4.10 μg m<sup>−3</sup>. In addition, we found cross-validation <i>R</i><sup>2</sup> ranging from 0.62 to 0.78, MPE from 2.00 to 3.01 μg m<sup>−3</sup>, and RMSPE from 3.12 to 5.00 μg m<sup>−3</sup>, indicating a good agreement between the estimated and observed values. Spatial trends showed that high PM<sub>2.5</sub> levels occurred in urban areas and along major highways, while low concentrations appeared in rural or mountainous areas. Our time-series analysis showed that, for the 10-year study period, the PM<sub>2.5</sub> levels in the southeastern US have decreased by ~20%. The annual decrease has been relatively steady from 2001 to 2007 and from 2008 to 2010 while a significant drop occurred between 2007 and 2008. An observed increase in PM<sub>2.5</sub> levels in year 2005 is attributed to elevated sulfate concentrations in the study area in warm months of 2005.http://www.atmos-chem-phys.net/14/6301/2014/acp-14-6301-2014.pdf
collection DOAJ
language English
format Article
sources DOAJ
author X. Hu
L. A. Waller
A. Lyapustin
Y. Wang
Y. Liu
spellingShingle X. Hu
L. A. Waller
A. Lyapustin
Y. Wang
Y. Liu
10-year spatial and temporal trends of PM<sub>2.5</sub> concentrations in the southeastern US estimated using high-resolution satellite data
Atmospheric Chemistry and Physics
author_facet X. Hu
L. A. Waller
A. Lyapustin
Y. Wang
Y. Liu
author_sort X. Hu
title 10-year spatial and temporal trends of PM<sub>2.5</sub> concentrations in the southeastern US estimated using high-resolution satellite data
title_short 10-year spatial and temporal trends of PM<sub>2.5</sub> concentrations in the southeastern US estimated using high-resolution satellite data
title_full 10-year spatial and temporal trends of PM<sub>2.5</sub> concentrations in the southeastern US estimated using high-resolution satellite data
title_fullStr 10-year spatial and temporal trends of PM<sub>2.5</sub> concentrations in the southeastern US estimated using high-resolution satellite data
title_full_unstemmed 10-year spatial and temporal trends of PM<sub>2.5</sub> concentrations in the southeastern US estimated using high-resolution satellite data
title_sort 10-year spatial and temporal trends of pm<sub>2.5</sub> concentrations in the southeastern us estimated using high-resolution satellite data
publisher Copernicus Publications
series Atmospheric Chemistry and Physics
issn 1680-7316
1680-7324
publishDate 2014-06-01
description Long-term PM<sub>2.5</sub> exposure has been associated with various adverse health outcomes. However, most ground monitors are located in urban areas, leading to a potentially biased representation of true regional PM<sub>2.5</sub> levels. To facilitate epidemiological studies, accurate estimates of the spatiotemporally continuous distribution of PM<sub>2.5</sub> concentrations are important. Satellite-retrieved aerosol optical depth (AOD) has been increasingly used for PM<sub>2.5</sub> concentration estimation due to its comprehensive spatial coverage. Nevertheless, previous studies indicated that an inherent disadvantage of many AOD products is their coarse spatial resolution. For instance, the available spatial resolutions of the Moderate Resolution Imaging Spectroradiometer (MODIS) and the Multiangle Imaging SpectroRadiometer (MISR) AOD products are 10 and 17.6 km, respectively. In this paper, a new AOD product with 1 km spatial resolution retrieved by the multi-angle implementation of atmospheric correction (MAIAC) algorithm based on MODIS measurements was used. A two-stage model was developed to account for both spatial and temporal variability in the PM<sub>2.5</sub>–AOD relationship by incorporating the MAIAC AOD, meteorological fields, and land use variables as predictors. Our study area is in the southeastern US centered at the Atlanta metro area, and data from 2001 to 2010 were collected from various sources. The model was fitted annually, and we obtained model fitting <i>R</i><sup>2</sup> ranging from 0.71 to 0.85, mean prediction error (MPE) from 1.73 to 2.50 μg m<sup>−3</sup>, and root mean squared prediction error (RMSPE) from 2.75 to 4.10 μg m<sup>−3</sup>. In addition, we found cross-validation <i>R</i><sup>2</sup> ranging from 0.62 to 0.78, MPE from 2.00 to 3.01 μg m<sup>−3</sup>, and RMSPE from 3.12 to 5.00 μg m<sup>−3</sup>, indicating a good agreement between the estimated and observed values. Spatial trends showed that high PM<sub>2.5</sub> levels occurred in urban areas and along major highways, while low concentrations appeared in rural or mountainous areas. Our time-series analysis showed that, for the 10-year study period, the PM<sub>2.5</sub> levels in the southeastern US have decreased by ~20%. The annual decrease has been relatively steady from 2001 to 2007 and from 2008 to 2010 while a significant drop occurred between 2007 and 2008. An observed increase in PM<sub>2.5</sub> levels in year 2005 is attributed to elevated sulfate concentrations in the study area in warm months of 2005.
url http://www.atmos-chem-phys.net/14/6301/2014/acp-14-6301-2014.pdf
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