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Unusually cold conditions in Arctic winter 2010/11 led to large stratospheric ozone loss. We investigate this with UV‐visible measurements made at Eureka, Canada (80.05°N, 86.42°W) from 1999–2011. For 8–22 March 2011, OClO was enhanced, indicating chlorine activation above Eureka. Ozone columns were lower than in any other year in the record, reaching minima of 237 DU and 247 DU in two datasets. The average NO2 column inside the vortex, measured at visible and UV wavelengths, was 46 ± 30% and 45 ± 27% lower in 2011 than the average NO2column from previous years. Ozone column loss was estimated from two ozone datasets, using a modeled passive ozone tracer. For 12–20 March 2011, the average ozone loss was 27% and 29% (99 DU and 108 DU). The largest percent ozone loss in the 11‐year record of 47% (250 DU and 251 DU) was observed on 5 April 2011.

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A new gas chromatographic method developed to quantitatively determine important atmospheric halocarbons is described. Target compounds include replacement CFCs, chlorinated solvents, and biosynthesized (naturally produced) organohalogens, all trace gases in the atmosphere at concentrations ranging from 0.1 to 600 pptv (where pptv = 1 part in 10(-)(12) by volume). A combination of ultralow concentrations and relatively small electron attachment cross sections renders these compounds very difficult to routinely measure in the background air typical of remote atmospheric monitoring stations. Detection is achieved by preconcentration of a 200-mL air sample using an adsorbent-filled microtrap and enhancement of electron capture detector response by oxygen doping one of two detectors connected in series. Oxygen doping specifically targets halocarbons with relatively poor electron attachment rate coefficients. The work described here details construction of a novel analytical system, laboratory trials, and optimization followed by an extended field campaign at a remote atmospheric monitoring station, Mace Head, Ireland. A calibration standard or ambient air sample was acquired every hour using a cyclic, automated procedure without employing cryogenic preconcentration or refocusing. Overall precision of the analytical method for the target compounds is between 0.3 and 1.5%.

No abstract