PubMed2005
Juvenile sheepshead minnows Cyprinodon variegatus were exposed to the explosive compounds 2,4,6-trinitrotoluene (TNT), hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX), octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX) and to the TNT transformation products 2-aminodinitrotoluene (2-ADNT) and 2,4-diaminonitrotoluene (2,4-DANT) in five separate water-only experiments. A one-compartment model was used to characterize uptake (k(u)) and elimination (k(e)) rate constants and to estimate bioconcentration factors (BCFs). The compounds investigated in this study are weakly hydrophobic. Kinetically derived BCFs (9.6, 13.1, 0.5, 1.7, and 0.5 ml g(-1) for TNT, 2-ADNT, 2,4-DANT, RDX, and HMX, respectively) confirmed the expected low bioaccumulative potential of those compounds and the positive relationship between log BCF and log K(ow) (1.6, 2.0, 0.8, 0.9, and 0.2 for TNT, 2-ADNT, 2,4-DANT, RDX, and HMX, respectively). The uptake clearance (k(u)) was relatively slow for all compounds (7.3, 12.6, 1.3, 0.15, and 0.06 ml g(-1)h(-1) for TNT, 2-ADNT, 2,4-DANT, RDX, and HMX, respectively), and overall, it decreased with decreasing compound hydrophobicity. Elimination was extremely fast for the nitroaromatic compounds (0.77, 0.96, and 2.74 h(-1) for TNT, 2-ADNT, and 2,4-DANT, respectively), thus resulting in very short biological half-lives (<1 hour), but it was much slower for the cyclonitramines (0.09 h(-1) for RDX and 0.12 h(-1) for HMX). Although ADNTs were present in fish exposed to TNT, the parent compound was the dominant compound in tissues during the uptake and elimination exposures. The rates of metabolite formation (0.06 h(-1)) and elimination (0.16 h(-1)) were much slower than the rate of elimination of the parent compound (0.80 h(-1)). Because of the fast elimination rate of TNT and its transformation products and the exceedingly low bioaccumulative potential of RDX and HMX, exposure conditions likely associated with the presence of explosives in aquatic systems are unlikely to pose unacceptable risks to fish.