Ml. Bertho et al., THE LEAD CONTENT OF ATMOSPHERIC AEROSOLS ABOVE THE EASTERN CHANNEL - SEASONAL VARIABILITY AND SOLUBILITY IN A COASTAL SEAWATER, Hydrobiologia, 374, 1998, pp. 317-332
In order to describe the seasonal variability of the atmospheric lead
concentrations above the Eastern Channel, aerosols samples have been c
ollected by bulk filtration at the Cape Gris-Nez (Dover Strait) during
one year. A statistical analysis of the obtained time-series from lea
d concentrations and rain amounts illustrates the geochemical implicat
ions of a scavenging process: when precipitations become lower than th
e average rain events, the lead concentrations become higher than the
mean values and reciprocally. On a global scale, the lead concentratio
ns over the Eastern Channel and the Southern Eight of the North Sea ha
ve decreased by about one order of magnitude since fifteen years. Lead
concentrations have been compared to the origin of the collected air
masses. The use of the back-trajectories permits us to classify the or
igins of the air masses among five geographical sectors relevant to th
e position of our sampling site: Atlantic Ocean and English Channel; N
orth Sea; British Islands; Southern and Western Europe; Scandinavia an
d Central Europe. Continental sectors show greater lead concentrations
than marine and semi-continental sectors, by a factor of about 3 to 7
. These results are in a good agreement with the assumption according
to which the atmospheric lead is mainly associated with emissions from
heavy industrialised and urbanised areas, especially from automotive
origin. Under our experimental conditions, the solubility in a coastal
seawater for 'continental' lead is different from the one of 'maritim
e' lead. These dissolution experiments are developed in order to ultim
ately answer to the questions 'how does the dry fall-out scatter into
the upper layer of the seawater mass, regarding as a chemical system?'
and more particularly 'what is the part of the heavy metals transport
ed via the atmosphere which is rapidly transferred into the dissolved
phase, i.e. under a labile form potentially available for the interfac
ial organisms?'.