Phytoextraction of heavy metals from a multiply contaminated dredged sediment by chicory (Cichorium intybus L.) and castor bean (Ricinus communis L.) enhanced with EDTA, NTA, and citric acid application.

The remediation of contaminated dredged sediments is necessary to eliminate the risk towards human beings or the environment when there is disposal on land. A greenhouse experiment was carried out to evaluate the chemically assisted phytoextraction to clean up dredged sediment contaminated with Cr, Cu, Pb, and Zn. The ability of castor bean and chicory to absorb, translocate, and accumulate metals from sediment to root and shoot was evaluated by applying EDTA (5 mM), NTA (5 mM), and citric acid (60 mM) to sediment, before the harvest. Citric acid 60 mM was the most effective treatment in increasing Cr, Cu, and Pb in castor bean and chicory shoot. Chicory could accumulate 1730 mg Cr kg-1 in shoot, and had greater values than one for the bioaccumulation and translocation factors when citric acid was added to the sediment. But, the Cr percentages removed per harvest of chicory were 0.05% and were lower for Cu, Pb, and Zn due to low biomass obtained. Citric acid-assisted phytoextraction with chicory can be a promising short time solution to reduce Cr concentration in sediment and reach the Cr level guide for industrial land use only if suitable agronomic practices could be implemented to increase crop yield.

Failure of long-distance movement of southern bean mosaic virus in a resistant host is correlated with lack of normal virion formation.

Sunn-hemp mosaic tobamovirus (SHMV) facilitated the spread of the cowpea strain of southern bean sobemovirus (SBMV-C) only in inoculated leaves of common bean (Phaseolus vulgaris L. cv. Bountiful), a resistant host for SBMV-C. Tissue prints of bean primary leaves doubly inoculated with SHMV and SBMV-C, developed by Western blotting, showed the presence of the SBMV-C capsid antigen in the mesophyll and epidermis, but no antigen was detected in the conducting bundles. Typical SBMV-C virions were not seen in electron micrographs of immunogold-labelled mesophyll cells; instead, specifically labelled, amorphous protein clumps were found in the vacuole. Particles of smaller diameter than that of typical SBMV-C virions were specifically trapped by SBMV antibodies following immunosorbent electron microscopy of extracts from doubly infected leaves. SBMV-C coat protein from infected Vigna unguiculata L. (cowpea) and bean plants showed no difference in its mobility following electrophoresis in denaturing SDS-polyacrylamide gels. Lack of efficient assembly of SBMV-C virions does not impede cell-to-cell movement of the virus in doubly infected leaves of bean, yet it is probably an important factor in determining the inability of SBMV-C to move into and/or through the vascular system of this host.