The partition coefficients and sorption capacities for cadmium, copper
, and lead in freshwater sediments are derived from fitting a Langmuir
isotherm to data from 14 sediments. The metal activity in the solutio
n phase was measured using specific ion electrodes. The metal sorption
due to acid-volatile sulfide was subtracted from the total sorbed met
al to produce the metal bound to other sediment phases. Organic carbon
normalized isotherms provide a reasonable representation of the metal
sorption. Partition coefficients and capacities are calculated for pH
= 6, 7, and 8 (for Cd). The organic carbon normalized isotherm parame
ters for the sediments are compared to those reported for soils and sl
udges. The comparisons for cadmium exhibit differences for which no re
ady explanations are available. For copper and lead, however, the diff
erences can be attributed to the use of specific ion electrodes for me
asuring metal activity in the sediment experiments. The cadmium sedime
nt partition coefficients contribute a small increment to the sediment
quality criteria. For copper and lead, however, the additional bindin
g to sediment organic carbon is significant and can amount to 1 to 10
and 10 to 100 mu mol/g dry weight for lead and copper, respectively, d
epending on the organic carbon concentration of the sediment.