Abstract

An important decrease in the level of stratospheric ozone has been observed during the past decade (1), with accompanying increases in UV-B radiation (2) and some UV-A radiation (3), thus leading to probable damage to aquatic and terrestrial ecosystems (4–7). Inhabitants of terrestrial and aquatic ecosystems have developed strategies to cope with the potential stress induced by UV radiation. One of these strategies is the synthesis of photoprotector compounds derived mainly from the biosynthetic route of the polymalonate acetate (8–13). As levels of UV radiation increase, accumulation rates of some photoprotective compounds in lichen species from the Chilean Alpine zones also increase (14). Photodegradation of depsides may have accounted for the low levels of phenolics in lichens at higher elevations (15). It was observed that, in Xanthoparmelia lichens from the Alpine regions of Chile, the higher the altitude where the lichen was found, the greater amount of usnic acid it produced (16). This increase of usnic acid is the result of the lichen’s ability to adapt to radiation, which ensures its survival in extreme environmental conditions. In thalli from Xanthoparmelia oleosa collected at 4690 m no usnic acid was detected, which could be proof of the presence of a photodegradation product of usnic acid (17) but which has not been identified to date. In growth-chamber experiments lasting 1 week, thalli of Umbilicaria americana always produced smaller amounts of phenolic residue when exposed to both UV-B and UV-A radiation, compared with exposure to UV-A alone. In one field experiment exclusion of UV-B by light filtration produced significant increases in phenolic compounds. This increase occurs only during spring and autumn, when lichens are metabolically more active (18). In this article we evaluated the accumulation rates of usnic acid in Xanthoparmelia microspora (Mull. Arg. Hale) exposed to doses of solar radiation and to additional doses of UV-A and UV-B radiation. Furthermore, we report on the photolysis of usnic acid in nonnucleofilic solvents during exposure to higher doses of UV-A and UV-B radiation.

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