Ptant, Cell and Environment (^997) 20,[982][983][984][985][986][987][988][989][990][991][992][993][994],viv In this range, solute mobilities increased up to 1000-fold, which corresponds to temperature coefficients Qio of 3 (IAA in P. armeniaca) to 14 (cholesterol in fi. hetix). For most species, Arrhenius graphs showed good linearity up to 40 °C, and up to 78 °C for some species, while for others activation energies declined with increasing temperature. However, no distinct phase transitions caused by sudden structural changes in the CM were observed. In three species we examined whether heating to 70 °C changed solute mobility irreversibly by comparing Arrhenius graphs for two successive experiments with the same CM. The two graphs were very similar for P, taurocerasus, while mobilities in the second graph were somewhat reduced for C. aurantium and greatly increased (at 25 and 35 °C) for H. helix. This indicates rearrangements of at least some wax constituents when heated to high temperatures. The activation energies of diffusion (/i|,) ranged from 75 to 189 k. F moP' depending on .species and .solute size. Size selectivity and variability between cuticles decreased witb increasing temperature, and this is caused by differences in li|,. An excellent correlation between the pre-exponential factor of the Arrhenius equation and /i,, was observed, which is evidence that organic solutes differing greatly in molecular size (130-349 cm' moP') and cuticle/water partition coefficient (25-10*") use similar diffusion paths in the CM of all 12 plant species tested. Diffusion occurs in regions with identical phy.sicochemical properties and differs only in magnitude.