Abstract. Simultaneous in situ measurements of the long-lived trace species N20, CH4, CFC-12, CFC-113, CFC-11, CC14, CH3CC13, H-1211, and SF6 were made in the lower stratosphere and upper troposphere on board the NASA ER-2 high-altitude aircraft during the 1994 campaign Airborne Southern Hemisphere Ozone Experiment/Measurements for Assessing the Effects of Stratospheric Aircraft. The observed extratropical tracer abundances exhibit compact mutual correlations that show little interhemispheric difference or seasonal variability except at higher altitudes in southern hemisphere spring. The environmental impact of the measured source gases depends, among other factors, on the rate at which they release ozone-depleting chemicals in the stratosphere, that is, on their stratospheric lifetimes. We calculate the mean age of the air from the SF 6 measurements and show how stratospheric lifetimes of the other species may be derived semiempirically from their observed gradients with respect to mean age at the extratropical tropopause. We also derive independent stratospheric lifetimes using the CFC-11 lifetime and the slopes of the tracer' s correlations with CFC-11. In both cases, we correct for the influence of tropospheric growth on stratospheric tracer gradients using the observed mean age of the air, time series of observed tropospheric abundances, and model-derived estimates of the width of the stratospheric age spectrum. Lifetime results from the two methods are consistent with each other. Our best estimates for stratospheric lifetimes are 122 + 24 years for N2 ¸, 93 + 18 years for CH4, 87 + 17 years for CFC-12, 100 + 32 years for CFC-113, 32 + 6 years for CC14, 34 + 7 years for CH3CC13, and 24 + 6 years for H-1211. Most of these estimates are significantly smaller than currently recommended lifetimes, which are based largely on photochemical model calculations. Because the derived stratospheric lifetimes are identical to atmospheric lifetimes for most of the species considered, the shorter lifetimes would imply a faster recovery of the ozone layer following the phaseout of industrial halocarbons than currently predicted.

The Tropospheric Emission Spectrometer (TES) on the Earth Observing System (EOS)‐Aura spacecraft measures global profiles of atmospheric ozone with vertical resolution of 6–7 km in the troposphere for the nadir view. For a first validation of TES ozone measurements we have compared TES‐retrieved ozone profiles to ozonesondes from fall, 2004. In some cases the ozonesonde data are from dedicated launches timed to match the Aura overpass, while other comparisons are performed with routine data available from the Southern Hemisphere Additional Ozonesonde (SHADOZ) archive and World Ozone and Ultraviolet Data Center (WOUDC) data archives. We account for TES measurement sensitivity and vertical resolution by applying the TES‐averaging kernel and constraint to the ozonesonde data before differencing the profiles. Overall, for V001 data, TES ozone profiles are systematically higher than sondes in the upper troposphere but compare well in the lower troposphere, with respect to estimated errors. These comparisons show that TES is able to detect relative variations in the coarse vertical structure of tropospheric ozone.

Movie S1Movie S1. Results of the assimilation of OCO-2 XCO2 data into a high-resolution global model for March 2015 through July 2015, highlighting the springtime reduction in atmospheric CO2.

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CH4 and N2O are useful as dynamical tracers of stratospheric air transport because of their long photochemical lifetimes over a wide range of altitudes. The cryogenic limb array etalon spectrometer (CLAES) instrument on the NASA UARS provided simultaneous global measurements of the altitude profiles of CH4 and N2O mixing ratios in the stratosphere between October 1, 1991, and May 5, 1993. Data between January 9, 1992, and May 5, 1993 (388 days), have been processed using version 7 data processing software, and this paper is concerned with the assessment of the quality of this data set. CLAES is a limb‐viewing emission instrument, and approximately 1200 profiles were obtained each 24‐hour period for each constituent over a nominal altitude range of 100 to 0.1 mbar (16 to 64 km). Each latitude was sampled 30 times per day between latitudes 34°S and 80°N, or 34°N and 80°S depending on the yaw direction of the UARS, and nearly all local times were sampled in about 36 days. This data set extends the altitude, latitude, and seasonal coverage of previous experiments, particularly in relation to measurements at high winter latitudes. To arrive at estimates of experiment error, we compared CLAES profiles for both gases with a wide variety of correlative data from ground‐based, rocket, aircraft, balloon, and space‐borne sensors, looked at the repeatability of multiple profiles in the same location, and carried out empirical estimates of experiment error based on knowledge of instrument characteristics. These analyses indicate an average single‐profile CH4 systematic error of about 15% between 46 and 0.46 mbar, with CLAES biased high. The CH4 random error over this range is 0.08 to 0.05 parts per million, which translates to about 7% in the midstratosphere. For N2O the indicated systematic error is less than 15% at all altitudes between 68 and 2 mbar, with CLAES tending to be high below 6.8 mbar and low above. The N2O random error is 20 to 5 ppb between 46 and 2 mbar, which also translates to 7% in the low to midstratosphere. Both tracers have useful profile information to as low as 68 mbar, excluding the tropics, and as high as 0.2 mbar (CH4) and 1 mbar (N2O). The global fields show generally good spatial correlation and exhibit the major morphological and seasonal features seen in previous global field data. Several morphological features are pointed out for regions and conditions for which there have been essentially no previous data. These include the differential behavior of the tracer isopleths near and inside the Antarctic winter vortex, and local maxima in the tropics in 1992, probably associated with the Mount Pinatubo sulfate aerosol layer. Overall, the results of this validation exercise indicate that the version 7 CH4 and N2O data sets can be used with good confidence for quantitative and qualitative studies of stratospheric and lower‐mesospheric atmospheric structure and dynamics.