Relative contributions of fossil and contemporary carbon sources to PM 2.5 aerosols at nine Interagency Monitoring for Protection of Visual Environments (IMPROVE) network sites

被引:44
作者
Bench, Graham
Fallon, Stewart
Schichtel, Bret
Malm, William
McDade, Charles
机构
[1] Lawrence Livermore Natl Lab, Ctr Accelerator Mass Spectrometry, Livermore, CA 94551 USA
[2] Colorado State Univ, Cooperat Inst Res Atmosphere, Natl Pk Serv, Ft Collins, CO 80523 USA
[3] Univ Calif Davis, Crocker Nucl Lab, Davis, CA 95616 USA
关键词
D O I
10.1029/2006JD007708
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
[1] Particulate matter aerosols contribute to haze diminishing vistas and scenery at national parks and wilderness areas within the United States. To increase understanding of the sources of carbonaceous aerosols at these settings, the total carbon loading and C-14/C ratio of PM 2.5 aerosols at nine Interagency Monitoring for Protection of Visual Environments ( IMPROVE) network sites were measured. Aerosols were collected weekly in the summer and winter at one rural site, two urban sites, five sites located in national parks and one site located in a wildlife preserve. The carbon measurements together with the absence of C-14 in fossil carbon materials and known C-14/C levels in contemporary carbon materials were used to derive contemporary and fossil carbon contents of the particulate matter. Contemporary and fossil carbon aerosol loadings varied across the sites and suggest different percentages of carbon source inputs. The urban sites had the highest fossil carbon loadings that comprised around 50% of the total carbon aerosol loading. The wildlife preserve and national park sites together with the rural site had much lower fossil carbon loading components. At these sites, variations in the total carbon aerosol loading were dominated by nonfossil carbon sources. This suggests that reduction of anthropogenic sources of fossil carbon aerosols may result only in little decrease in carbonaceous aerosol loading at many national parks and rural areas. Examination of the major sources of uncertainty that might cause contemporary carbon contents to be artificially high indicates that potential errors and biases in the methodology do not change the fundamental conclusions of this study.
引用
收藏
页数:10
相关论文
共 26 条
  • [21] Trumbore S, 2000, ECOL APPL, V10, P399, DOI 10.1890/1051-0761(2000)010[0399:AOSOMA]2.0.CO
  • [22] 2
  • [23] Trumbore S., 2002, EOS T AGU, V83, P267, DOI DOI 10.1029/2002E0000187
  • [24] Trumbore S. E., 2002, EOS T AM GEOPHYS UN, V83, P265, DOI DOI 10.1029/2002EO000187
  • [25] *US EPA, 1997, FED REGISTER, V62, P1
  • [26] Source apportionment of PM2.5 in the southeastern United States using solvent-extractable organic compounds as tracers
    Zheng, M
    Cass, GR
    Schauer, JJ
    Edgerton, ES
    [J]. ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2002, 36 (11) : 2361 - 2371