While biomagnification of certain organic contaminants in food chains has b
een observed in field studies, the mechanism of the biomagnification proces
s is still unresolved. Knowledge of the mechanism by which contaminants are
absorbed and biomagnified in food chains is important in environmental ris
k assessment and studies of chemical bioavailability. In this study, we hyp
othesize a fugacity based model of the gastrointestinal absorption of conta
minants. We test the model in a 73 day laboratory, gastrointestinal magnifi
cation study of 2,2',4,4',6,6'-hexachlorobiphenyl in adult rainbow trout (O
ncorhynchus mykiss) and in a field study of the gastrointestinal magnificat
ion of PCB congeners in rock bass (Ambloplites rupestris). Both studies sho
w that the fugacity of the test chemicals in the gastrointestinal tract (GI
T) can increase to levels up to 7-8-fold greater than those in the consumed
food. The fugacity increase in the GIT is the result of a drop in the chym
e's fugacity capacity for the test chemicals (i.e. approximately 4-fold in
this study) and an increase in chemical concentration due to food absorptio
n in the GIT (i.e. approximately 2-fold in this study). Food digestibility
and absorption are found to be critical factors controlling biomagnificatio
n factors and dietary uptake efficiencies under laboratory and field condit
ions.