John G Watson

Dr. John G Watson

orcid

Research Focus & Metrics

Academic Career Length

53Years (1974-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 June 1993 in Atmospheric Environment. Part A. General Topics
Verified
Journal Article
Closed access
JCJudith C. Chow
Judith C. Chow
JWJohn G Watson
John G Watson
LPLyle C. Pritchett
Lyle C. Pritchett
WPWilliam R. Pierson
William R. Pierson
CFClifton A. Frazier
Clifton A. Frazier
RPRichard G. Purcell
Richard G. Purcell

1 September 2007 in Journal of the Air & Waste Management Association
Verified
Journal Article
Closed access
JCJudith C. Chow
Judith C. Chow
JWJohn G Watson
John G Watson
LCLung-Wen Antony Chen
Lung-Wen Antony Chen
MCM.C. Oliver Chang
M.C. Oliver Chang
NRNorman F. Robinson
Norman F. Robinson
SKSteven Kohl
Steven Kohl
Thermally derived carbon fractions including organic carbon (OC) and elemental carbon (EC) have been reported for the U.S. Interagency Monitoring of PROtected Visual Environments (IMPROVE) network ...

1 June 2002 in Journal of the Air & Waste Management Association
Verified
Journal Article
Closed access
JWJohn G Watson
John G Watson
The 1999 Regional Haze Rule provides a context for this review of visibility, the science that describes it, and the use of that science in regulatory guidance. The scientific basis for the 1999 regulation is adequate. The deciview metric that tracks progress is an imperfect but objective measure of what people see near the prevailing visual range. The definition of natural visibility conditions is adequate for current planning, but it will need to be refined as visibility improves. Emissions from other countries will set achievable levels above those produced by natural sources. Some natural events, notably dust storms and wildfires, are episodic and cannot be represented by annual average background values or emission estimates. Sulfur dioxide (SO2) emission reductions correspond with lower sulfate (SO4 2−) concentrations and visibility im-provements in the regions where these have occurred. Non-road emissions have been growing more rapidly than emissions from other sources, which have remained stable or decreased since 1970. Simpler models representing transport, limiting precursor pollutants, and gas-to-particle equilibrium should be used to understand where and when emission reductions will be effective, rather than large complex models that have insufficient input and validation measurements. Examples of model-based source attribution show large differences among estimates from various modeling systems and with ambient measurements.

20 July 2004 in Environmental Science & Technology
Verified
Journal Article
Closed access
JCJudith C. Chow
Judith C. Chow
JWJohn G Watson
John G Watson
LCLung-Wen Antony Chen
Lung-Wen Antony Chen
WAW. Patrick Arnott
W. Patrick Arnott
Hans MoosmullerHans Moosmuller
Hans Moosmuller
KFKochy Fung
Kochy Fung

22 November 2005 in Atmospheric Chemistry and Physics
Verified
Journal Article
Open access
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JCJunji Cao
Junji Cao
FWF. Wu
F. Wu
JCJ. C. Chow
J. C. Chow
Shuncheng LeeShuncheng Lee
Shuncheng Lee
YLY. Li
Y. Li
SLS. X. Liu
S. X. Liu
Continuous measurements of atmospheric organic and elemental carbon (OC and EC) were taken during the high-pollution fall and winter seasons at Xi'an, Shaanxi Province, China from September 2003 through February 2004. Battery-powered mini-volume samplers collected PM2.5 samples daily and PM10 samples every third day. Samples were also obtained from the plumes of residential coal combustion, motor-vehicle exhaust, and biomass burning sources. These samples were analyzed for OC/EC by thermal/optical reflectance (TOR) following the Interagency Monitoring of Protected Visual Environments (IMPROVE) protocol. OC and EC levels at Xi'an are higher than most urban cities in Asia. Average PM2.5 OC concentrations in fall and winter were 34.1±18.0 μg m−3 and 61.9±;33.2 μg m−3, respectively; while EC concentrations were 11.3±6.9 μg m−3 and 12.3±5.3 μg m−3, respectively. Most of the OC and EC were in the PM2.5 fraction. OC was strongly correlated (R>0.95) with EC in the autumn and moderately correlated (R=0.81) with EC during winter. Carbonaceous aerosol (OC×1.6+EC) accounted for 48.8%±10.1% of the PM2.5 mass during fall and 45.9±7.5% during winter. The average OC/EC ratio was 3.3 in fall and 5.1 in winter, with individual OC/EC ratios nearly always exceeding 2.0. The higher wintertime OC/EC corresponded to increased residential coal combustion for heating. Total carbon (TC) was associated with source contributions using absolute principal component analysis (APCA) with eight thermally-derived carbon fractions. During fall, 73% of TC was attributed to gasoline engine exhaust, 23% to diesel exhaust, and 4% to biomass burning. During winter, 44% of TC was attributed to gasoline engine exhaust, 44% to coal burning, 9% to biomass burning, and 3% to diesel engine exhaust.

1 June 2001 in Chemosphere
Verified
Journal Article
Closed access
JWJohn G Watson
John G Watson
JCJudith C Chow
Judith C Chow
JHJames E Houck
James E Houck