An air quality observatory was operated at a rural site on the Mediter
ranean coast of Israel near the ancient city of Caesarea between May 1
993 and October 1995. The objective of the study was to monitor transp
ort of air pollutants from remote sources that arrive at the Israeli c
oast. Normally, under onshore westerly winds, which come from the Medi
terranean sea, the levels of NO, NOy and SO2 at the site dropped to be
low 0.5 ppbv, CO to below 150 ppbv, and the O-3 levels ranged between
30 and 60 ppbv. During the last week of October 1993, an unusual serie
s of pollution episodes occurred, with elevated values for all the pol
lutants being recorded during onshore hows. The SO2 concentration reac
hed 30 ppbv, NO and NOy more than 100 ppbv and O-3 levels rose above 2
00 ppbv. On 26 October the O-3 levels were the highest observed with a
n abnormally high concentration of 230 ppbv being recorded. The episod
e that occurred on that day was investigated in detail in order to und
erstand the cause for this high ozone value. During the above day, nig
ht and early morning, easterly winds swept the air parcels containing
the locally emitted pollution westwards over the sea. The intense phot
ochemical activity that occurred while the air mass was over the sea f
or a relatively extensive time combined with the low mixing height on
that day and the fact that the returning air mass reached the measurin
g site at peak ozone formation time, give rise to record ozone levels.
The elevated concentrations were measured when the polluted air parce
ls returned to the coast during the afternoon onshore flows. An excell
ent linear correlation between O-3 and NOy was obtained for the time p
eriod between 1400 and 1700. The linear fit between O-3 and NOy indica
tes that approximately 11 O-3 molecules were formed for each NOy molec
ule present. Similar ratios have been reported in other studies dealin
g with aged air masses under NOy limited conditions. (C) 1997 Elsevier
Science Ltd.