Pd. Goldan et al., HYDROCARBON MEASUREMENTS IN THE SOUTHEASTERN UNITED-STATES - THE RURAL OXIDANTS IN THE SOUTHERN ENVIRONMENT (ROSE) PROGRAM 1990, JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 100(D12), 1995, pp. 25945-25963
An automated gas chromatographic system was employed at a rural site i
n western central Alabama to measure atmospheric hydrocarbons and oxyg
enated hydrocarbons (oxy-hydrocarbons) on an hourly basis from June 8
to July 19, 1990. The location, which was a designated site for the So
uthern Oxidant Study (SOS), was instrumented for a wide variety of mea
surements allowing the hydrocarbon and oxy-hydrocarbon measurements to
be interpreted both in terms of meteorological data and as part of a
large suite of gas phase measurements. Although the site is situated i
n a Loblolly pine plantation, isoprene was observed to be the dominant
hydrocarbon during the daytime with afternoon maxima of about 7 parts
per billion by volume (ppbv). Decrease of isoprene after sunset was t
oo rapid to be accounted for solely on the basis of gas phase chemistr
y. During the nighttime, alpha-pinene and beta-pinene were the dominan
t hydrocarbons of natural origin. The ratio of alpha-pinene to beta-pi
nene showed a well-defined diurnal pattern, decreasing by more than 30
% during the night; a decrease that could be understood on the basis o
f local gas phase chemistry. Oxy-hydrocarbons, dominated by methanol a
nd acetone, were the most abundant compounds observed. On a carbon ato
m basis, the oxy-hydrocarbons contributed about 46% of the measured at
mospheric burden during the daytime and about 40% at night. The simila
rity of the observed diurnal methanol variation to that of isoprene an
d subsequent measurements [McDonald and Fall, 1993] indicate that much
of the observed methanol was of local biogenic origin. Correlation of
acetone with methanol suggests that it, also, has a significant bioge
nic source. In spite of the site's rural location, anthropogenic hydro
carbons constituted, on a carbon atom basis, about 21% of the hydrocar
bon burden measured during the daytime and about 55% at night. Signifi
cant diurnal variations of the anthropogenic hydrocarbons, with increa
ses at night, appeared to be driven by the frequent formation of a sha
llow nocturnal boundary layer.