Effects of simulated solar radiation on the bioaccumulation of polycyclic aromatic hydrocarbons by the duckweed Lemna gibba

Abstract

AbstractLight (particularly ultraviolet B) results in photomodification of polycyclic aromatic hydrocarbons (PAHs) to products with increased polarity and water solubility and enhanced toxicity relative to the parent compounds. The uptake and depuration kinetics of three representative PAHs, anthracene (ANT), phenanthrene (PHE), and benzo [a]pyrene (BAP), and their photomodified products were determined for Lemna gibba. The 14C‐labeled PAHs were delivered to the plants in their aqueous growth medium either via a dimethylsulfoxide (DMSO) carrier or adsorbed directly to sand placed in the medium. Assimilation was carried out under simulated solar radiation (SSR) and in darkness. The potential sites of PAH action within the plants were defined by identifying the subcellular location of both intact and photomodified PAHs following assimilation. Lemna gibba had a high capacity for intact ANT, PHE, and BAP in the dark regardless of the two routes of delivery. Depuration was also rapid. Net assimilation of all three PAHs in the dark was always higher when the chemicals were delivered with DMSO than from sand, although first‐order kinetics were apparent with both delivery systems. The relative levels of assimilation were PHE > ANT > BAP. Polycyclic aromatic hydrocarbons were rapidly assimilated under SSR, albeit net assimilation for both the intact and photomodified forms was generally lower under SSR compared with darkness. This was also reflected in the bioconcentration factors, which were highest in darkness for each PAH and dropped significantly under SSR and after photomodification. Both intact and photooxidized PAHs accumulated preferentially in the thylakoids and microsomes of L. gibba, suggesting these to be the subcellular compartments most at risk from PAH damage.