Simultaneous measurements of UV irradiance have been made from two adj
acent sites (47.5 degrees N, 11.1 degrees E) in Garmisch-Partenkirchen
(730m a.s.l.) and the Zugspitze (2964m a.s.l.). New maximum erythemal
ly weighted irradiance levels were observed in Garmisch-Partenkirchen,
Germany during March 1996 and June 1995. The March episode was associ
ated with a polar stratospheric cloud while the June episode was assoc
iated with an unusually low total ozone column (for June) and broken c
louds. The June maximum may be especially significant because it was p
receded by a minimum of UV irradiance caused by heavy cloud cover, thu
s the absolute change in the UV irradiance was very extreme. Even thou
gh the maximum irradiance levels increased, these measurements show th
at the monthly mean spectral UV irradiation over Germany in 1995 was n
ot significantly different compared to previous years. This is importa
nt because an increase in the number of extreme fluctuations from low
UV irradiation followed by very high UV irradiation may be much more d
angerous for the biosphere than a small gradual increase in average UV
dose, because natural adaptation mechanisms may not be able to cope w
ith these extreme fluctuations. The monthly erythemally weighted irrad
iation is between 25 and 90% higher on the Zugspitze than on the lower
Garmisch-Partenkirchen site. The difference between the two sites can
not be characterized by a single number because the average monthly ra
tio of the irradiances was very variable with respect to both time and
wavelength. The variability in the differences between the two sites
indicates that the differences are caused by a combination of several
factors including Rayleigh scattering, cloud effects, air pollutants (
e.g. tropospheric ozone), aerosols and albedo. These results show that
although UV irradiation measurements from one site (e.g. Garmisch-Par
tenkirchen) can be used in the assessment of biological effects in the
immediate neighbourhood, data from a single site are not sufficient t
o extrapolate even to different altitudes near the measurement site an
d certainly should not be used to extrapolate conclusions to the atmos
pheric chemistry of the global troposphere. (C) 1997 Elsevier Science
Ltd.