Sammendrag
Abstract: Increased anthropogenic emissions of nitrogen oxides, carbon monoxide, volatile organic compounds and methane causes production of ozone in the troposphere, particularly in the northern hemisphere. This causes warming of the northern hemisphere troposphere as tropospheric ozone acts as a greenhouse gas. Ozone depletion events (ODEs) caused by reactive halogens in the Arctic are a well known and thoroughly studied phenomena, which may modulate the warming effect of tropospheric ozone in the Arctic. The purpose of this thesis is to develop a reliable halogen-chemistry scheme in the Oslo CTM3 and estimate performance of the new scheme by comparing with observations and the original CTM3. The ozone-induced radiative forcing (RF) due to the implemented halogen chemistry can then be estimated. The new scheme was run for 2001 and 2013, but only the 2001 run was compared with observations. The new scheme shows no significant correlation with ground-based measurements of ozone. In the new scheme, \chem{HBr} appears to be the dominant halogen species during and after ODEs. The halogen-induced ozone depletion in the new scheme works, but it causes too much ozone depletion. Diverging results in the 2001- and 2013-run makes it impossible to conclude any horizontal or vertical dependence regarding tropospheric ozone-induced RF with regards to the new halogen implementation. The temporally (February to June) and globally averaged RF due to tropospheric ozone yielded by the BE-branch demonstrates large deviations between the 2001-run, RF $=-0.012\pm0.12$ Wm$^{-2}$, and the 2013-run, RF $= 0.45\pm0.42$ Wm$^{-2}$. Due to the inconsistency in RF and the fact that the present-day and pre-industrial setup of the BE-branch, these estimates are not correct. The new scheme does not sufficiently reproduce the observed ODEs in the Arctic, and the RF-estimates are variable and inconsistent. Further development of the halogen chemistry is needed to estimate the effect on ozone-induced RF in the troposphere.