It is likely that Polylepis (Rosaceae) occurs naturally at higher elevations than any other arborescent angiosperm genus in the world. The 15 species (Simpson 1979) are confined to the South American Andes where they occur primarily in tropical alpine environments. Some Polylepis species tend to form discrete forest stands reaching elevations over 5000 m, well above the upper continuous forest limit (timberline). Throughout their high altitude distribution most members of this genus are exposed to rigorous climatic conditions in which diurnal temperature variations by far exceed seasonal ones and night frosts are frequent. The genus is exclusively arborescent (trees or shrubs), with individuals ranging in height from 1 m to no more than 30 m. The trees tend to have twisted, crooked stems and branches, particularly in open, exposed habitats. The form and branching pattern of some individuals resembles those of krummholz trees found in temperate alpine regions. The bark is deep red in color and consists of several layers of thin, exfoliating sheets. Although the exfoliating bark is particularly thick at the base of the stem or large branches, the insulating effect is by no means comparable to that of the marcescent leaves that surround the stem of the adjacent giant rosette plants (Smith 1979; Goldstein & Meinzer 1983). The leaves are compound and alternate but often appear whorled owing to the compression of internodes at the branch tips. The leaflets are small, dark green above and are covered with dense, silvery trichomes on the underside in several species. An extensive documentation of leaf anatomy and several important species-specific characters of potential adaptive value such as the degree of deciduousness is to be found in Simpson's (1979) revision. Polylepis trees seldom grow as isolated individuals. They tend to form