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Observation of halogen species in the Amundsen Gulf, Arctic, by active long-path differential optical absorption spectroscopy

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TLDR
Measurements of halogen oxides performed in the Amundsen Gulf, Arctic, during spring 2008 indicate the presence of reactive chlorine in the Arctic boundary layer and an observed linear decrease of maximum bromine oxide levels with ambient temperature during sunlight provides indications on the conditions required for the emission of RHS.
Abstract
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.

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Citations
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Journal ArticleDOI

Tropospheric Halogen Chemistry: Sources, Cycling,and Impacts

TL;DR: Reactive halogen species are potent oxidizers for organic and inorganic compounds throughout the troposphere and are powerful climate forcing agents through direct and indirect radiative effects.
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Reactive halogen chemistry in the troposphere

TL;DR: This critical review summarises the current understanding and uncertainties of the main halogen photochemistry processes, including the current knowledge of the atmospheric impact of halogen chemistry as well as open questions and future research needs.
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Riverine source of Arctic Ocean mercury inferred from atmospheric observations

TL;DR: The authors showed that human activities, including industry and mining, have increased inorganic mercury deposition in terrestrial and aquatic ecosystems, and model simulations indicate that circumpolar rivers deliver large quantities of mercury to the Arctic Ocean during summer.
References
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Journal ArticleDOI

Evaluated kinetic and photochemical data for atmospheric chemistry

TL;DR: A critical evaluation of the kinetics and photochemistry of gas phase chemical reactions of neutral species involved in middle atmosphere chemistry (10-55 km altitude) was carried out by the authors under the auspices of the CODATA Task Group on Chemical Kinetics.
Journal ArticleDOI

Ozone destruction and photochemical reactions at polar sunrise in the lower Arctic atmosphere

TL;DR: In this paper, the authors focus on recent ground-level observations from the Canadian baseline station at Alert (82.5° N, 62.3° W) and from aircraft that show that ozone destruction is occurring under the Arctic surface radiation inversion during March and April as the Sun rises.
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