In the polar tropospheric boundary layer, reactive halogen species (RHS) are responsible for ozone depletion as well as the oxidation of elemental mercury and dimethyl sulphide. After polar sunrise, air masses enriched in reactive bromine cover areas of several million square kilometers. Still, the source and release mechanisms of halogens are not completely understood. We report measurements of halogen oxides performed in the Amundsen Gulf, Arctic, during spring 2008. Active long-path differential optical absorption spectroscopy (LP-DOAS) measurements were set up offshore, several kilometers from the coast, directly on the sea ice, which was never done before. High bromine oxide concentrations were detected frequently during sunlight hours with a characteristic daily cycle showing morning and evening maxima and a minimum at noon. The, so far, highest observed average mixing ratio in the polar boundary layer of 41 pmol/mol (equal to pptv) was detected. Only short sea ice contact is required to release high amounts of bromine. An observed linear decrease of maximum bromine oxide levels with ambient temperature during sunlight, between −24°C and −15°C, provides indications on the conditions required for the emission of RHS. In addition, the data indicate the presence of reactive chlorine in the Arctic boundary layer. In contrast to Antarctica, iodine oxide was not detected above a detection limit of 0.3 pmol/mol.halogen chemistry | ozone depletion | bromine explosion | polar | DOAS T he depletion of the stratospheric ozone layer due to reactive halogen species is well known. Similarly, ozone depletion events (ODEs) in the polar boundary layer, arising after sunrise, were discovered in the 1980s (1, 2, 3). These events were found to be related to high concentrations of filterable bromine. It was therefore proposed that ozone could be destroyed by catalytic reaction cycles involving bromine atoms (Br) and bromine monoxide (BrO) (4).The initial reaction is the release of Br 2 from the liquid to the gas phase and the photolysis to Br, which will lead to a quick oxidation to BrO by destroying an ozone molecule. Note that there is always some production of Br atoms from the photochemical degradation of CH 3 Br, which is ubiquitous in the atmosphere. Bromine atoms are recycled from BrO by different processes. The most important recycling is the BrO self-reaction (R 2·BrO ) with the total rate constant k 2·BrO ¼ 3.2 × 10 −12 cm 3 molec −1 s −1 (5) producing Br atoms or Br 2 . During daylight, Br 2 is again photolyzed to Br, thus all channels of R 2·BrO lead to a net loss of O 3 . Overall, reactive bromine (Br and BrO) acts as a catalyst for ozone destruction. An autocatalytic release of bromine from the sea salt surface ice, the so-called "bromine explosion" (6), supplies sufficient bromine to the gas phase. A simplified overview on bromine release mechanisms and ozone destruction cycles is given in Fig. 1 (for a recent review see 7).The key role of bromine was first confirmed by long-path differential optical absorption ...