The equilibrium partitioning of tetrachloromethane (CCl4), trichloroet
hene (C2HCl3), tetrachloroethene (C2Cl4) and 1,1,1-trichloroethane (C2
H3Cl3) between the gas phase and both needles and hexane-extractable l
eaf waxes of Scots pine (Pinus sylvestris L.) was measured at room tem
perature (20 degrees C). Needles and wax came to equilibrium with gas-
phase concentrations in the range 2.5-1500 mg m(-3) within 6 hours. Pa
rtition ratios (PR: g mg(-3) needle/g m(-3) gaseous nitrogen) for whol
e needles were 9, 27, 200 and 10 for CCl4, C2HCl3, C2Cl4 and C2H3Cl3 r
espectively; for extractable wax the partition ratios were 90, 390, 21
00 and 950 respectively. The partition ratios are similar to published
data for Norway spruce. There was a linear relationship between log(P
R) for whole needles and the octanol-air equilibrium constant, log(K-o
a), suggesting that the PR depends on the balance between the octanol-
water equilibrium constant and aqueous solubility. There was also a li
near relationship between log(PR) and boiling point for the 4 chlorina
ted hydrocarbons studied. (C) 1998 Elsevier Science Ltd.