The concentrations of total gaseous mercury (Hg) were determined at hourly
intervals along with relevant environmental parameters that include both me
teorological plus criteria pollutant data during two field campaigns (Septe
mber 1997 and May/June 1998). The mean concentrations of Hg for the two stu
dy periods were computed as 3.94 and 3.43 ng m(-3), respectively. By separa
ting the data into daytime and nighttime periods, we further analyzed diurn
al variation patterns for both seasons. Using our Hg data sets, we were abl
e to recognize two contrasting diurnal variation patterns of Hg between two
different seasons that can be characterized as: (1) the occurrences of pea
k Hg concentration during daytime (fall) and (2) slight reductions in dayti
me Hg concentration relative to nighttime (summer). To study the systematic
differences in diurnal patterns between two different seasons, we analyzed
Hg data in terms of different statistical approaches such as correlation (
and linear regression) and factor analysis. Results of these analyses consi
stently indicated that different mechanisms were responsible for controllin
g the daytime distribution patterns of Hg. When the relationship between Hg
and concurrently determined O-3 is considered, its reaction with ozone is
unlikely to limit Hg levels as the dominant sink mechanism (within the rang
es of ozone concentrations found during this study, regardless of season).
It is on the other hand suspected that the variation of boundary layer cond
itions between day/night periods may have been important in introducing the
relative reduction in daytime Hg levels during summer. To further provide
a general account of short-term variations in Hg distribution data, it is d
esirable to describe other unknown sink mechanisms. (C) 2000 Elsevier Scien
ce Ltd. All rights reserved.