Aerosol elemental carbon measurements were taken at two rural sites in southwestern Pennsylvania during August 1983. Carbon, though a small part of the aerosol mass at both sites, was a leading constituent of the aerosol on an atom basis. Time-weighted average concentrations at Allegheny Mountain and Laurel Hill were 1.2 and 1.4 [mu]g m-3, respectively. Absolute Principal Component Analysis followed by multiple regression and Chemical Mass Balance techniques were utilized to apportion the measured elemental carbon to its sources. Motor vehicles were estimated to be the largest source of elemental carbon at the two sites, contributing 41-68% and 34-56% at Allegheny Mountain and Laurel Hill, respectively.Peer Reviewedhttp://deepblue.lib.umich...
The identification of different sources of the carbonaceous aerosol (organics and black carbon) was ...
An intensive investigation of carbonaceous PM2.5 and TSP from Pudong (China) was conducted as part o...
A study was conducted to quantify wintertime contributions of source types to carbonaceous PM2.5 at ...
Two fundamentally different techniques for measuring atmospheric elemental carbon (EC) aerosol were ...
Particulate matter aerosols contribute to haze diminishing vistas and scenery at National Parks and ...
While recent advances in instrumentation permit routine determination of elemental carbon concentrat...
This study was conducted at a site adjacent to the I-710 freeway in Long Beach California from March...
A fine particle air monitoring network was operated in the Los Angeles area during 1982. It was foun...
Particulate matter aerosols contribute to haze diminishing vistas and scenery at national parks and ...
We measured the radiocarbon isotope signals in various fractions of carbonaceous aerosols sampled ac...
We use a global three-dimensional model (GEOS-CHEM) to better quantify the sources of elemental carb...
An intensive investigation of carbonaceous PM2.5 and TSP (total suspended particles) from Pudong (Ch...
Continuous measurements of atmospheric organic and elemental carbon (OC and EC) were taken during th...
Both organic carbon (OC) and elemental carbon (EC) were measured during PRIDE-PRD 2006 summer campai...
March 1999.Also issued as Lorraine Calame's thesis (M.S.) -- Colorado State University, 1999.Include...
The identification of different sources of the carbonaceous aerosol (organics and black carbon) was ...
An intensive investigation of carbonaceous PM2.5 and TSP from Pudong (China) was conducted as part o...
A study was conducted to quantify wintertime contributions of source types to carbonaceous PM2.5 at ...
Two fundamentally different techniques for measuring atmospheric elemental carbon (EC) aerosol were ...
Particulate matter aerosols contribute to haze diminishing vistas and scenery at National Parks and ...
While recent advances in instrumentation permit routine determination of elemental carbon concentrat...
This study was conducted at a site adjacent to the I-710 freeway in Long Beach California from March...
A fine particle air monitoring network was operated in the Los Angeles area during 1982. It was foun...
Particulate matter aerosols contribute to haze diminishing vistas and scenery at national parks and ...
We measured the radiocarbon isotope signals in various fractions of carbonaceous aerosols sampled ac...
We use a global three-dimensional model (GEOS-CHEM) to better quantify the sources of elemental carb...
An intensive investigation of carbonaceous PM2.5 and TSP (total suspended particles) from Pudong (Ch...
Continuous measurements of atmospheric organic and elemental carbon (OC and EC) were taken during th...
Both organic carbon (OC) and elemental carbon (EC) were measured during PRIDE-PRD 2006 summer campai...
March 1999.Also issued as Lorraine Calame's thesis (M.S.) -- Colorado State University, 1999.Include...
The identification of different sources of the carbonaceous aerosol (organics and black carbon) was ...
An intensive investigation of carbonaceous PM2.5 and TSP from Pudong (China) was conducted as part o...
A study was conducted to quantify wintertime contributions of source types to carbonaceous PM2.5 at ...