EVALUATION OF A COMPREHENSIVE EULERIAN AIR-QUALITY MODEL WITH MULTIPLE CHEMICAL-SPECIES MEASUREMENTS USING PRINCIPAL COMPONENT ANALYSIS

被引:7
作者
LI, SM
ANLAUF, KG
WIEBE, HA
BOTTENHEIM, JW
PUCKETT, KJ
机构
[1] Atmospheric Environment Service, Downsview, Ont. M3H 5T4
关键词
EULERIAN MODEL; PRINCIPAL COMPONENT ANALYSIS; MODEL EVALUATION; AIR QUALITY;
D O I
10.1016/1352-2310(94)90004-3
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Using a principal component analysis technique and data on atmospheric gases and aerosols at a rural site in Ontario, Canada from the Eulerian model evaluation field study (EMEFS), the Eulerian acid deposition and oxidant model (ADOM) is evaluated. Seventy-nine and 76% of the variances in the data and model output, respectively, are explained by three principal components. They are a chemically aged/transported component, a diurnal cycle component, and an area emission component, all characterized by their ratios of gases and temporal variation patterns. The ADOM component contributions to sulphur species are in general agreement with the EMEFS components, but with notable differences for key photochemical species including O-3. The temporal variations of the ADOM components are close to those of the EMEFS components. The EMEFS chemically aged/transported component shows a high degree of photochemical processing, with the ratios [NOx]/[TNOy]=0.3 and [O-3]/([TNOy]-[NOx])=9+/-1. The corresponding ADOM component predicts lower [NOx]/[TNOy] and [O-3]/([TNOy]-[NOx]) ratios, probably caused by a chemical mechanism in the model that is too fast, and lower contributions to O-3, NO2, TNO3, PAN, TNOy, and HCHO, probably caused by model grid dilution or lower model emissions. The EMEFS diurnal component owes its variance to the daily photochemistry and nighttime dry deposition of the chemical species. In comparison, the matching ADOM component underpredicts the ratio [O-3]/([TNOy]-[NOx]) and the NO2 consumption and O-3 production but overpredicts the contributions to the other species. The EMEFS emission component represents emissions from local/regional area sources. The corresponding ADOM component underpredicts TNOy by 44% and the fraction of TNOy as NOx compared to the EMEFS component, suggesting that the model has lower emissions of NOx and a photochemical mechanism that converts NOx faster than indicated by the EMEFS results.
引用
收藏
页码:3449 / 3461
页数:13
相关论文
共 34 条
[1]   A DETERMINATION OF THE SOURCES OF AIRBORNE PARTICLES COLLECTED DURING THE REGIONAL AIR-POLLUTION STUDY [J].
ALPERT, DJ ;
HOPKE, PK .
ATMOSPHERIC ENVIRONMENT, 1981, 15 (05) :675-687
[2]  
BAILEY EM, 1994, IN PRESS J GEOPHYS R
[3]  
BRICE K A, 1988, Tellus Series B Chemical and Physical Meteorology, V40, P408
[4]   ASSESSMENT OF POLLUTANT EMISSION INVENTORIES BY PRINCIPAL COMPONENT ANALYSIS OF AMBIENT AIR MEASUREMENTS [J].
BUHR, MP ;
TRAINER, M ;
PARRISH, DD ;
SIEVERS, RE ;
FEHSENFELD, FC .
GEOPHYSICAL RESEARCH LETTERS, 1992, 19 (10) :1009-1012
[5]   A 3-DIMENSIONAL EULERIAN ACID DEPOSITION MODEL - PHYSICAL CONCEPTS AND FORMULATION [J].
CHANG, JS ;
BROST, RA ;
ISAKSEN, ISA ;
MADRONICH, S ;
MIDDLETON, P ;
STOCKWELL, WR ;
WALCEK, CJ .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1987, 92 (D12) :14681-14700
[6]   THE EVALUATION OF ACID DEPOSITION MODELS USING PRINCIPAL COMPONENT SPACES [J].
COHN, RD ;
DENNIS, RL .
ATMOSPHERIC ENVIRONMENT, 1994, 28 (15) :2531-2543
[7]   A NUMERICAL EXPERIMENT ON THE RELATIVE IMPORTANCE OF H2O2 AND O3 IN AQUEOUS CONVERSION OF SO2 TO SO42- [J].
FUNG, CS ;
MISRA, PK ;
BLOXAM, R ;
WONG, S .
ATMOSPHERIC ENVIRONMENT PART A-GENERAL TOPICS, 1991, 25 (02) :411-423
[8]   COVARIATIONS IN THE CONCENTRATIONS OF ORGANIC-COMPOUNDS ASSOCIATED WITH SPRINGTIME ATMOSPHERIC AEROSOLS [J].
GREAVES, RC ;
BARKLEY, RM ;
SIEVERS, RE ;
MEGLEN, RR .
ATMOSPHERIC ENVIRONMENT, 1987, 21 (12) :2549-2561
[9]  
HANSEN DA, 1990, 7TH P AMS JOINT C AP, P58
[10]   ATMOSPHERIC AEROSOL FACTOR MODELS, MASS AND MISSING DATA [J].
HEIDAM, NZ .
ATMOSPHERIC ENVIRONMENT, 1982, 16 (08) :1923-1931