Radiocarbon measurement of the biogenic contribution to summertime PM-2.5 ambient aerosol in Nashville, TN

Radiocarbon (14C) measurements performed on PM-2.5 samples collected near Nashville, TN from June 21 to July 13, 1999, showed high levels of modern carbon, ranging from 56% to 80% of the total carbon in the samples. Radiocarbon measurements performed on dichloromethane extracts of a subset of the samples showed modern carbon levels that were on average only 9% smaller than those for total carbon. A new approach based on the Chapman–Richards model of tree growth was used to define the quantitative relationship between measurements of `percent modern carbon' and inferred `percent biogenic carbon'. The results of this study contribute to a growing body of evidence (including measurements of radiocarbon, organic carbon to elemental carbon ratios and organic tracer species, as well as results from chemical mass balance and air quality simulation modeling) in support of the importance of biogenic secondary organic aerosol in the Southeastern US during summer.

[1]  J. Huntzicker,et al.  Secondary formation of organic aerosol in the Los Angeles basin: A descriptive analysis of organic and elemental carbon concentrations , 1991 .

[2]  I. Levin,et al.  RADIOCARBON - A UNIQUE TRACER OF GLOBAL CARBON CYCLE DYNAMICS , 2000 .

[3]  L. A. Currie,et al.  Accelerator mass spectrometric determination of carbon-14 in the low-polarity organic fraction of atmospheric particles , 1990 .

[4]  Graham Bench,et al.  Measurement of contemporary and fossil carbon contents of PM2.5 aerosols: results from Turtleback Dome, Yosemite National Park. , 2004, Environmental science & technology.

[5]  C. Lewis,et al.  Biogenic contributions to atmospheric volatile organic compounds in Azusa, California , 2002 .

[6]  K. Rennolls,et al.  Timber Management-A Quantitative Approach. , 1984 .

[7]  D. Grosjean Solvent extraction and organic carbon determination in atmospheric particulate matter: the organic extraction-organic carbon analyzer (OE-OCA) technique. , 1975, Analytical chemistry.

[8]  S. Pandis,et al.  Evaluation of secondary organic aerosol formation in winter , 1999 .

[9]  Judith C. Chow,et al.  Comparison of IMPROVE and NIOSH Carbon Measurements , 2001 .

[10]  D. Donahue,et al.  Radiocarbon measurements at the University of Arizona AMS facility , 1990 .

[11]  R. Draxler,et al.  Meteorological Factors of Ozone Predictability at Houston, Texas , 2000, Journal of the Air & Waste Management Association.

[12]  R. Gerlach,et al.  Radiocarbon: nature's tracer for carbonaceous pollutants , 1982 .

[13]  W. Parkhurst,et al.  Fossil Sources of Ambient Aerosol Carbon Based on 14C Measurements Special Issue of Aerosol Science and Technology on Findings from the Fine Particulate Matter Supersites Program , 2004 .

[14]  Christian Seigneur,et al.  Uncertainties in modeling secondary organic aerosols: three-dimensional modeling studies in Nashville/western Tennessee. , 2003, Environmental science & technology.

[15]  F. J. Richards A Flexible Growth Function for Empirical Use , 1959 .

[16]  B. Simoneit,et al.  Identification and emission factors of molecular tracers in organic aerosols from biomass burning Part 1. Temperate climate conifers , 2001 .

[17]  Michael O. Rodgers,et al.  Analysis of motor vehicle emissions during the Nashville/Middle Tennessee Ozone Study , 2001 .

[18]  Robert K. Stevens,et al.  Contribution of woodsmoke and motor vehicle emissions to ambient aerosol mutagenicity. , 1988, Environmental science & technology.

[19]  M. Stuiver International Agreements and the Use of the New Oxalic Acid Standard , 1983, Radiocarbon: An International Journal of Cosmogenic Isotope Research.

[20]  R. Cary,et al.  Elemental Carbon-Based Method for Monitoring Occupational Exposures to Particulate Diesel Exhaust , 1996 .

[21]  B. Turpin,et al.  Origins of primary and secondary organic aerosol in Atlanta: results of time-resolved measurements during the Atlanta Supersite Experiment. , 2002, Environmental science & technology.

[22]  Edward O. Edney,et al.  Polar organic oxygenates in PM2.5 at a southeastern site in the United States , 2003 .

[23]  J. Schauer,et al.  Source apportionment of PM2.5 in the Southeastern United States using solvent-extractable organic compounds as tracers. , 2002, Environmental science & technology.

[24]  H. Synal,et al.  Radiocarbon (14C)-deduced biogenic and anthropogenic contributions to organic carbon (OC) of urban aerosols from Zürich, Switzerland , 2004, Atmospheric Environment.

[25]  D. Allen,et al.  Fine particulate matter source attribution for Southeast Texas using 14C/13C ratios , 2002 .