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UCATS (the UAS Chromatograph for Atmospheric Trace Species) was designed and built for observations of important atmospheric trace gases from unmanned aircraft systems (UAS) in the upper troposphere and lower stratosphere (UT/LS). Initially it measured major chlorofluorocarbons (CFCs) and the stratospheric transport tracers nitrous oxide (N2O) and sulfur hexafluoride (SF6), using gas chromatography with electron capture detection. Compact ozone (O3) and water vapor (H2O) instruments were added to enhance science missions on platforms with relatively small payloads. Over the past decade, UCATS has been reconfigured to measure methane (CH4), carbon monoxide (CO), and molecular hydrogen (H2) instead of CFCs and has undergone numerous upgrades to its subsystems. It has served as part of large payloads on stratospheric UAS missions to probe the tropical tropopause region and transport of air into the stratosphere, in piloted aircraft studies of greenhouse gases, transport, and chemistry in the troposphere, and will soon return to the study of stratospheric ozone depletion, one of the original goals for UCATS. Each deployment brought different challenges, which were largely met or resolved. The design, capabilities, modifications and some results from UCATS are shown and described here, including changes for upcoming missions.

The United States government has operated Dobson ozone spectrophotometers at various sites, starting during the International Geophysical Year (1 July 1957 to 31 December 1958). A network of stations for long-term monitoring of the total column content (thickness of the ozone layer) of the atmosphere was established in the early 1960s and eventually grew to 16 stations, 14 of which are still operational and submit data to the United States of America's National Oceanic and Atmospheric Administration (NOAA). Seven of these sites are also part of the Network for the Detection of Atmospheric Composition Change (NDACC), an organization that maintains its own data archive. Due to recent changes in data processing software the entire dataset was re-evaluated for possible changes. To evaluate and minimize potential changes caused by the new processing software, the reprocessed data record was compared to the original data record archived in the World Ozone and UV Data Center (WOUDC) in Toronto, Canada. The history of the observations at the individual stations, the instruments used for the NOAA network monitoring at the station, the method for reducing zenith-sky observations to total ozone, and calibration procedures were re-evaluated using data quality control tools built into the new software. At the completion of the evaluation, the new datasets are to be published as an update to the WOUDC and NDACC archives, and the entire dataset is to be made available to the scientific community. The procedure for reprocessing Dobson data and the results of the reanalysis on the archived record are presented in this paper. A summary of historical changes to 14 station records is also provided.

Extracting globally representative trend information from lower tropospheric ozone observations is extremely difficult due to the highly variable distribution and interannual variability of ozone, and the ongoing shift of ozone precursor emissions from high latitudes to low latitudes. Here we report surface ozone trends at 27 globally distributed remote locations (20 in the Northern Hemisphere, 7 in the Southern Hemisphere), focusing on continuous time series that extend from the present back to at least 1995. While these sites are only representative of less than 25% of the global surface area, this analysis provides a range of regional long-term ozone trends for the evaluation of global chemistry-climate models. Trends are based on monthly mean ozone anomalies, and all sites have at least 20 years of data, which improves the likelihood that a robust trend value is due to changes in ozone precursor emissions and/or forced climate change rather than naturally occurring climate variability. Since 1995, the Northern Hemisphere sites are nearly evenly split between positive and negative ozone trends, while 5 of 7 Southern Hemisphere sites have positive trends. Positive trends are in the range of 0.5–2 ppbv decade–1, with ozone increasing at Mauna Loa by roughly 50% since the late 1950s. Two high elevation Alpine sites, discussed by previous assessments, exhibit decreasing ozone trends in contrast to the positive trend observed by IAGOS commercial aircraft in the European lower free-troposphere. The Alpine sites frequently sample polluted European boundary layer air, especially in summer, and can only be representative of lower free tropospheric ozone if the data are carefully filtered to avoid boundary layer air. The highly variable ozone trends at these 27 surface sites are not necessarily indicative of free tropospheric trends, which have been overwhelmingly positive since the mid-1990s, as shown by recent studies of ozonesonde and aircraft observations. The IAGOS program acknowledges the European Commission for its support of the MOZAIC project (1994–2003) the preparatory phase of IAGOS (2005–2013) and IGAS (2013–2016).

Data from ground-based ozone (O3) vertical profiling platforms operated during the FRAPPE/DISCOVER-AQ campaigns in summer 2014 were used to characterize key processes responsible for establishing O3 profile development in the boundary layer in the Northern Colorado Front Range. Morning mixing from the upper boundary layer and lower free troposphere into the lower boundary layer was the key process establishing the mid-morning boundary layer O3 mixing ratio. Photochemical O3 production throughout the boundary layer builds on the mid-morning profile. From late morning to mid-afternoon the continuing O3 increase was nearly uniform through the depth of the profile measured by the tethersonde (~400 m). Ozonesondes flown on a near daily schedule over a four week period with multiple profiles on a number of days captured the full 1500 to 2000 m vertical extent of O3 enhancements in the mixed boundary layer confirming O3 production throughout the entire boundary layer. Continuous O3 measurements from the Boulder Atmospheric Observatory (BAO) tall tower at 6 m and 300 m showed hourly O3 at the 6 m level ≥75 ppb on 15% of the days. The diurnal variation on these days followed a pattern similar to that seen in the tethersonde profiles. The association of high O3 days at the BAO tower with transport from sectors with intense oil and natural gas production toward the northeast suggests emissions from this industry were an important source of O3 precursors and are crucial in producing peak O3 events in the NCFR. Higher elevation locations to the west of the NCFR plains regularly experience higher O3 values than those in the lower elevation NCFR locations. Exposure of populations in these areas is not captured by the current regulatory network, and likely underestimated in population O3 exposure assessments.