During the past three years radiocarbon assay has emerged as a primary tool in the quantitative assignment of sources of urban and rural particulate pollution. Its use in several major field studies has come about because of its excellent (fossil/biogenic) discriminating power, because of advances in 14C measurements of small samples, and because of the increased significance of carbonaceous particles in the atmosphere. The problem is especially important in the cities, where increased concentrations of fine particles lead to pollution episodes characterized by poor visibility and changes in the radiation balance (absorption, scattering), and immediate and possibly long-term health effects. Efforts in source apportionment in such affected areas have been based on emissions inventories, dispersion modeling, and receptor modeling – ie, chemical and physical (and statistical) characterization of particles collected at designated receptor sites. It is in the last category that 14C has become quite effective in helping to resolve particle sources. Results are presented for studies carried out in Los Angeles, Denver, and Houston which incorporated 14C measurements, inorganic and organic chemical characterization, and receptor modeling. The 14C data indicated wide ranging contributions of biogenic and fossil carbon sources – eg, <10% to 60% contemporary (biogenic) in Houston – depending on meteorological, biological, and anthropological activity. The combined (chemical, isotopic, statistical) data point to sources such as vehicles, wood combustion, power plants, and vegetation.

Radiocarbon determinations, employing both decay and direct counting, were obtained on various organic fractions of four human skeletal samples previously assigned ages ranging from 28,000 to 70,000 years on the basis of their D/L aspartic acid racemization values. In all four cases, the 14C values require an order of magnitude reduction in age.

Huon pine is endemic to Tasmania. It has well-defined annual rings, may live for over 2000 years, and is particularly resistant to decay. Celery-top pine has similar characteristics and may live for 800 years. As part of a multi-disciplinary study of these trees and their habitat, a simple wood pretreatment method for isotope analysis is described. The solvent-acid-alkali-acid sequence yields a value of Delta-14C = -16 +/- 6% for AD 1941-45 Huon pine heartwood; Delta-4C for extracts containing various proportions of post-AD 1955 carbon are also presented. Delta-14C measurements on super-canopy and subcanopy leaves from Celery-top pines are compared and used to place an upper limit of 10% on the amount of sub-canopy CO2 assimilated by sapling leaves, originating from decaying litter-mass. 14C ages from well-preserved logs illustrate the potential for a continuous Holocene chronology from 7400 years BP to the present. A 12,000-year-old Celery-top log has also been found.

In recent years in California, smog aerosols have been observed in metropolitan and rural areas. We wondered what the relative contribution is from sources such as fossil fuel combustion (eg, cars, factories) and emissions from trees and other plants. Pollution produced by fossil fuel combustion can be distinguished from biological sources using radioactive carbon. Carbon in fossil organic materials is radioactively dead whereas carbon in living plants contains 14C. Smog particles were collected on clean glass or quartz fiber paper and analyzed in a small volume CO2 proportional counter for 14C content. Results are given for sampling locations at UCLA, El Monte, Riverside, and Lake Tahoe showing the relative contributions of fossil and modern carbon sources ranging from 0 to 74% and 26 to 100% respectively.

The extraction of dissolved carbonate species for age dating from a 100L water sample by the direct-precipitation method (DPM) and by the gas-evolution method (GEM) has been investigated. Stable carbon-isotope fractionation between initial and final carbon dioxide evolved was ca 11 per mil by GEM and 1 per mil by DPM. GEM will produce isotopically lighter carbon dioxide compared with DPM if carbonate recovery is low. Extraction efficiency of > 95% can be achieved by GEM in 3 hours using nitrogen gas at a sweeping rate of 2000cc per minute. DPM requires precipitates to settle overnight to assure > 95% recovery. GEM is little affected by a high concentration of sulfate ions, whereas DPM is greatly affected by sulfate resulting in less yield.