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
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作者:
Bench, Graham
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机构:Lawrence Livermore Natl Lab, Ctr Accelerator Mass Spectrometry, Livermore, CA 94551 USA
Bench, Graham
Fallon, Stewart
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机构:Lawrence Livermore Natl Lab, Ctr Accelerator Mass Spectrometry, Livermore, CA 94551 USA
Fallon, Stewart
Schichtel, Bret
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机构:Lawrence Livermore Natl Lab, Ctr Accelerator Mass Spectrometry, Livermore, CA 94551 USA
Schichtel, Bret
Malm, William
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机构:Lawrence Livermore Natl Lab, Ctr Accelerator Mass Spectrometry, Livermore, CA 94551 USA
Malm, William
McDade, Charles
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机构:Lawrence Livermore Natl Lab, Ctr Accelerator Mass Spectrometry, Livermore, CA 94551 USA
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
[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.
机构:
UNIV CALIF LOS ANGELES, INST GEOPHYS & PLANETARY PHYS, DEPT GEOG, LOS ANGELES, CA 90024 USAUNIV CALIF LOS ANGELES, INST GEOPHYS & PLANETARY PHYS, DEPT GEOG, LOS ANGELES, CA 90024 USA
BERGER, R
MCJUNKIN, D
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UNIV CALIF LOS ANGELES, INST GEOPHYS & PLANETARY PHYS, DEPT GEOG, LOS ANGELES, CA 90024 USAUNIV CALIF LOS ANGELES, INST GEOPHYS & PLANETARY PHYS, DEPT GEOG, LOS ANGELES, CA 90024 USA
MCJUNKIN, D
JOHNSON, R
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UNIV CALIF LOS ANGELES, INST GEOPHYS & PLANETARY PHYS, DEPT GEOG, LOS ANGELES, CA 90024 USAUNIV CALIF LOS ANGELES, INST GEOPHYS & PLANETARY PHYS, DEPT GEOG, LOS ANGELES, CA 90024 USA
机构:
UNIV CALIF LOS ANGELES, INST GEOPHYS & PLANETARY PHYS, DEPT GEOG, LOS ANGELES, CA 90024 USAUNIV CALIF LOS ANGELES, INST GEOPHYS & PLANETARY PHYS, DEPT GEOG, LOS ANGELES, CA 90024 USA
BERGER, R
MCJUNKIN, D
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UNIV CALIF LOS ANGELES, INST GEOPHYS & PLANETARY PHYS, DEPT GEOG, LOS ANGELES, CA 90024 USAUNIV CALIF LOS ANGELES, INST GEOPHYS & PLANETARY PHYS, DEPT GEOG, LOS ANGELES, CA 90024 USA
MCJUNKIN, D
JOHNSON, R
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UNIV CALIF LOS ANGELES, INST GEOPHYS & PLANETARY PHYS, DEPT GEOG, LOS ANGELES, CA 90024 USAUNIV CALIF LOS ANGELES, INST GEOPHYS & PLANETARY PHYS, DEPT GEOG, LOS ANGELES, CA 90024 USA