Study of the heavy metal phytoextraction capacity of two forage species growing in an hydroponic environment.

Sorghum and alfalfa are two important forage crops. We studied their capacity for accumulating heavy metals in hydroponic experiments. Cadmium, nickel (as divalent cations) and chromium (trivalent and hexavalent) were added individually to the nutrient solution in a range of concentrations from 1 to 80 mg/l. Cr(III) was complexed with EDTA to increase its bioavailability. In alfalfa the increases in the concentration of Cr(III) and Cr(VI) favoured translocation of the metals to the upper parts of the plants, while with Ni(II) the level of translocated metal remained almost unchanged. In sorghum, both Cr(VI) and Ni(II) produced similar results to those in alfalfa, but increases in the concentrations of Cd(II) and Cr(III) in the solution lead to a higher accumulation of the metal at the root level. The concentrations referred to the dry biomass of alfalfa were 500 mg/kg (aerial parts) and 1500 mg/kg (roots) of Cr(III), simultaneously enhancing plant growth. Sorghum captured 500 and 1100 mg/kg (in aerial parts) and 300 and 2000 mg/kg (in roots) for Ni(II) and Cd(II) respectively, without significant damage to its biomass. The results show that alfalfa and sorghum can not only grow in the presence of high heavy metal concentration but also capture and translocate them to the aerial parts; because of these results special attention should be given to these crop plants for their possible use in phytoremediation of large contaminated areas but especially to avoid the possible introduction of the metals accumulated in aerial parts into the food chain when those plants grow in contaminated areas.

Removal of azinphos methyl by alfalfa plants (Medicago sativa L.) in a soil-free system.

The objective of this study was to investigate the removal of azinphos methyl assisted by alfalfa plants, with special emphasis on the effects of this compound on some plant's physiological parameters. Hydroponic cultures of alfalfa (Medicago sativa L., var Romagnola) were employed as a model system. These cultures were exposed to a nutrient medium containing 10 mg/l of azinphos methyl. A first-order kinetic approach was used to describe the removal of azinphos methyl from the solution. After 20 days of culture, the initial amount of azinphos methyl was reduced to non-detectable levels in the presence of plants. In the absence of plants, 20% of azinphos methyl remained in the solution after 30 days of treatment. The half-life of the pesticide was reduced from 10.8 to 3.4 days in the presence of plants. The growth index of alfalfa plants exposed to azinphos methyl was negatively affected. Chlorophyll contents were reduced after 24 h of treatment and thereafter the levels were comparable to that of control plants. The peroxidase activity of alfalfa roots was not affected by the presence of azinphos methyl. In conclusion, alfalfa plants were able to survive when exposed to an effective concentration of 10 mg/l of azinphos methyl in the root zone, with some alterations on their physiological parameters.

Peroxidase production in vitro by Armoracia lapathifolia (horseradish)-transformed root cultures: effect of elicitation on level and profile of isoenzymes.

Transformed roots of Armoracia lapathifolia (horseradish) were established by infection with Agrobacterium rhizogenes LBA 9402. They were used as a culture system in vitro for peroxidase production in vitro, to avoid many of the problems that affect the traditional production from field-grown species of Armoracia sp. The time course of growth of these cultures showed that total peroxidase attained maximum levels at the end of the exponential growth phase. At this stage of culture, elicitation assays were performed with AgNO3 and CuSO4 as abiotic elicitors and with fungal extracts of Verticillum sp., Monodyctis cataneae and Aspergillus niger as biotic elicitors. The best results were obtained with Verticillum sp., 24 h after elicitation, with an increase of approx. 100% in peroxidase activity. The isoenzyme pattern analysed by isoelectric focusing revealed predominantly basic and acidic isoenzymes in both plant roots and transformed root cultures. Elicited samples showed a similar isoenzyme pattern with a slight increase in basic isoenzymes.