Modeled estimates of chlorpyrifos exposure and dose for the Minnesota and Arizona NHEXAS populations

被引:28
作者
Buck, RJ [1 ]
Özkaynak, H [1 ]
Xue, JP [1 ]
Zartarian, VG [1 ]
Hammerstrom, K [1 ]
机构
[1] US EPA, Off Res & Dev, Natl Exposure Res Lab, Res Triangle Pk, NC 27711 USA
来源
JOURNAL OF EXPOSURE ANALYSIS AND ENVIRONMENTAL EPIDEMIOLOGY | 2001年 / 11卷 / 03期
关键词
aggregate exposure; chlorpyrifos; exposure; model; NHEXAS;
D O I
10.1038/sj.jea.7500164
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
This paper presents a probabilistic, multimedia, multipathway exposure model and assessment for chlorpyrifos developed as part of the National Human Exposure Assessment Survey (NHEXAS). The model was constructed using available information prior to completion of the NHEXAS study. It simulates the distribution of daily aggregate and pathway-specific chlorpyrifos absorbed dose in the general population of the State of Arizona (AZ) and in children aged 3-12 years residing in Minneapolis-St. Paul, Minnesota (MSP). Pathways included were inhalation of indoor and outdoor air, dietary ingestion, non-dietary ingestion of dust and soil, and dermal contact with dust and soil. Probability distributions for model input parameters were derived from the available literature, and input values were chosen to represent chlorpyrifos concentrations and demographics in AZ and MSP to the extent possible. When the NHEXAS AZ and MSP data become available, they can be compared to the distributions derived in this and other prototype modeling assessments to test the adequacy of this pre-NHEXAS model assessment. Although pathway- specific absorbed dose estimates differed between AZ and MSP due to differences in model inputs between simulated adults and children, the aggregate model results and general findings for simulated AZ and MSP populations were similar. The major route of chlorpyrifos intake was food ingestion, followed by indoor air inhalation. Two-stage Monte Carlo simulation was used to derive estimates of both interindividual variability and uncertainty in the estimated distributions. The variability in the model results reflects the difference in activity patterns, exposure factors, and concentrations contacted by individuals during their daily activities. Based on the coefficient of variation, indoor air inhalation and dust ingestion were most variable relative to the mean, primarily because of variability in concentrations due to use or no-use of pesticides. Uncertainty analyses indicated a factor of 10-30 for uncertainty of model predictions of 10th, 50th, and 90th percentiles. The greatest source of uncertainty in the model stems from the definition of no household pesticide use as no use in the past year. Because chlorpyrifos persists in the residential environment for longer than a year, the modeled estimates are likely to be low. More information on pesticide usage and environmental concentrations measured at different post-application times is needed to refine and evaluate this and other pesticide exposure models.
引用
收藏
页码:253 / 268
页数:16
相关论文
共 60 条
[1]  
AHADAYA SM, 1981, PESTIC BIOCH PHYSL, V16, P38
[2]  
[Anonymous], 1935, The growth of the surface area of the human body
[4]  
BAKKE JE, 1976, J ENV SCI HLTH B, V3, P223
[5]   INTEGRATING UNCERTAINTY AND INTERINDIVIDUAL VARIABILITY IN ENVIRONMENTAL RISK ASSESSMENT [J].
BOGEN, KT ;
SPEAR, RC .
RISK ANALYSIS, 1987, 7 (04) :427-436
[6]   BIVARIATE DISTRIBUTIONS FOR HEIGHT AND WEIGHT OF MEN AND WOMEN IN THE UNITED-STATES [J].
BRAINARD, J ;
BURMASTER, DE .
RISK ANALYSIS, 1992, 12 (02) :267-275
[7]   Lognormal distributions for body weight as a function of age for males and females in the United States, 1976-1980 [J].
Burmaster, DE ;
Crouch, EAC .
RISK ANALYSIS, 1997, 17 (04) :499-505
[8]   PRELIMINARY ADULT SOIL INGESTION ESTIMATES - RESULTS OF A PILOT-STUDY [J].
CALABRESE, EJ ;
STANEK, EJ ;
GILBERT, CE ;
BARNES, RM .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 1990, 12 (01) :88-95
[9]   HOW MUCH SOIL DO YOUNG-CHILDREN INGEST - AN EPIDEMIOLOGIC-STUDY [J].
CALABRESE, EJ ;
BARNES, R ;
STANEK, EJ ;
PASTIDES, H ;
GILBERT, CE ;
VENEMAN, P ;
WANG, X ;
LASZTITY, A ;
KOSTECKI, PT .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 1989, 10 (02) :123-137
[10]  
CAMANN DE, 1994, ISEE ISEA JOINT ANN