Abstract
Based on the observed global concentrations of chloroform (CHCl3) in the air and seawater wedemonstrate that the tropical oceans are a source of chloroform to the atmosphere. Even thoughthe total yearly emissions of CHCl3, from the oceans are still uncertain, we estimate the flux to be 0.35 Tg yr-1. Anthropogenic sources we estimate to be 0.25 Tg yr-1. This result suggests thatatmospheric CHCl3, may be mostly natural in origin and not entirely man-made as previouslythought. The global burden of CHCl3, in the atmosphere is estimated to be about 0.33 Tg and itslifetime is about 6 months. Reaction with tropospheric OH radicals may explain most of theremoval of CHCI, from the atmosphere, but the likelihood of other removal mechanisms issuggested. An average concentration of about 25 ppt was observed at ground level, declining atabout 7% km-1 with height. The ratio of northern hemisphere to southern hemisphere burden of CHCl3, is found to be about 1.6. A global mass balance model is used to show that these findingsare mutually consistent.