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In vitro micropropagation of wild cherry is presently one of the main commercial ways to clonally propagate this species (Cornu and Boulay, 1986). In order to extend this technique to a large number of clones, it seems necessary to improve our knowledge of the behavior of the explants during the in vitro culture. Since plant growth regulators (PGR) play an important role in this technique (Margara, 1961 ), our attention was drawn to the effect of exo-

Internal levels of plant growth regulators during in vitro culture of wild cherry (Prunus avium L.)