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Total and cell wall-bound cadmium and the major antioxidants were measured in thalli of the lichen Xanthoria parietina (L.) Th. Fr. exposed to two Cd concentrations, namely 4.5 or 9.0 μm, in liquid medium during exposure periods of either 24 or 48 h. Total Cd in the thalli was within the range of previous field measurements and was proportional to the exposure concentration, but less than proportional with respect to exposure duration. More than half of the total Cd was immobilised by the cell wall. The adopted conditions of Cd stress caused: (i) no changes in dry weight and protein concentration; (ii) an increase in the level of ascorbic acid and a decrease in that of reduced glutathione, as well as an increase in guaiacol peroxidase activity; (iii) no changes or moderate decreases in the activities of superoxide dismutase, catalase, dehydroascorbate-, NADPH-dependent glutathione disulfide-, and monodehydroascorbate reductases and of ascorbate peroxidase; (iv) an increase of the level of thiobarbituric acid-reactive substances, assumed to reflect malondialdehyde formation arising from membrane lipid peroxidation. Thus, X. parietina might withstand realistic levels of Cd stress by: (1) intercepting the heavy metal at cell wall level, (2) the intervention of antioxidant metabolites, and (3) a moderate increase in guaiacol peroxidase activity.

Thalli of the lichen Xanthoria parietina (L.) Th. Fr. were soaked for either 24 or 48 h in a buffered medium in the presence of environmentally relevant concentrations (4.8 and 9.6 μM) of hexavalent chromium [Cr(VI)]. Treatment effects on the antioxidant status, differential distribution and fate of Cr(VI) among the mycobiont and the photobiont cells, and potential damage to cell ultrastructure in the two bionts, were evaluated. The adopted conditions of low Cr(VI) stress caused: (i) an increase in the level of ascorbic acid and a decrease in that of reduced glutathione, as well as a moderate increase in guaiacol peroxidase activity, only observed after treatment with 9.6 μM Cr(VI); (ii) no changes in malondialdehyde content; (iii) a remarkable Cr accumulation in the mycobiont cytosol and compartmentalisation in the mycobiont vacuoles;(iv) a modest apoplastic Cr immobilisation by the outer part of the cell walls, of both the mycobiont and the photobiont. The response of X.parietina to low concentrations of Cr(VI) appears to be a complex phenomenon, which might reflect maintenance of cellular homeostatic equilibria, rather than specific response pathways.