
A trajectory study into the origin of spring time Arctic boundary layer ozone depletion
Author(s) -
Bottenheim Jan W.,
Chan Elton
Publication year - 2006
Publication title -
journal of geophysical research: atmospheres
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.67
H-Index - 298
eISSN - 2156-2202
pISSN - 0148-0227
DOI - 10.1029/2006jd007055
Subject(s) - ozone depletion , ozone , atmospheric sciences , bromine , ozone layer , boundary layer , environmental science , stratosphere , chemistry , geology , meteorology , geography , physics , organic chemistry , thermodynamics
In polar regions, severe marine boundary layer ozone depletion episodes (ODEs) are a yearly recurring phenomenon in the spring. Using 9 years of 10‐day three‐dimensional trajectory calculations, the origin of ODEs at three Arctic observatories is investigated. The analysis indicates that marginal ice zones are potential source regions of ODEs. Those regions do broadly correspond to areas where increased levels of bromine oxide (BrO), an indicator of ozone depletion chemistry, are observed by the GOME satellite. The source region of ODEs, observed at Barrow, Alaska, is found to be about 1 day's travel upwind, in agreement with expectations based on the rate at which O 3 depletion chemistry occurs. In contrast, the likely source region for ODEs observed at Alert, Canada, and Zeppelinfjellet, Norway, appears to be located several days' travel upwind, off the Siberian coast. This result may reflect the absence of favorable ice conditions for O 3 depletion chemistry nearer those sites. Assuming that O 3 depletion occurs at those regions, this implies that air parcels without O 3 remain that way for several days or the depletion is slower than current understanding of the O 3 depletion chemistry suggests. Rapid changes in O 3 mole fractions at those measurement sites appears not to be an indication of fast chemical destruction of ozone but rather are due to abrupt air mass changes. Data for September indicate a much narrower distribution of ozone mole fractions and no particular pattern linking a preferred area with lower mole fractions.