Hannah Clark

Intraseasonal variations of water vapor in the tropical upper troposphere and tropopause region

We show the signature of the tropical intraseasonal oscillation (TIO) in upper tropospheric moisture and dynamical fields, roughly between 200 and 100 hPa. Relationships among these fields are examined using lag-correlation analysis and using multivariate extended empirical orthogonal functions (MEEOFs), which maximize the shared explained variance among several fields for both spatial and temporal variations. The MEEOFs show that all of the fields respond to the TIO and that the TIO is the dominant factor influencing each of the fields on these timescales. Convection associated with the TIO moistens the upper troposphere up to about 150 hPa, as expected; the behavior at 100 hPa is more complex. Over the longitude range where the TIO is associated with convection, roughly 60o-180oE, 100-hPa temperature and water vapor tend to be reduced above convection on TIO timescales. East of 180 o, though, the temperature and water vapor variations at 100 hPa become decoupled. The water vapor variations, like those of 200-hPa velocity potential, appear to speed up at about 180oE.

On the use of MOZAIC-IAGOS data to assess the ability of the MACC reanalysis to reproduce the distribution of ozone and CO in the UTLS over Europe

MOZAIC-IAGOS data are used to assess the ability of the MACC reanalysis (REAN) to reproduce distributions of ozone (O3) and carbon monoxide (CO), along with vertical and inter-annual variability in the upper troposphere/lower stratosphere region (UTLS) over Europe for the period 2003–2010. A control run (CNTRL, without assimilation) is compared with the MACC reanalysis (REAN, with assimilation) to assess the impact of assimilation. On average over the period, REAN underestimates ozone by 60 ppbv in the lower stratosphere (LS), whilst CO is overestimated by 20 ppbv. In the upper troposphere (UT), ozone is overestimated by 50 ppbv, while CO is partly over or underestimated by up to 20 ppbv. As expected, assimilation generally improves model results but there are some exceptions. Assimilation leads to increased CO mixing ratios in the UT which reduce the biases of the model in this region but the difference in CO mixing ratios between LS and UT has not changed and remains underestimated after assimilation. Therefore, this leads to a significant positive bias of CO in the LS after assimilation. Assimilation improves estimates of the amplitude of the seasonal cycle for both species. Additionally, the observations clearly show a general negative trend of CO in the UT which is rather well reproduced by REAN. However, REAN misses the observed inter-annual variability in summer. The O3–CO correlation in the Ex-UTLS is rather well reproduced by the CNTRL and REAN, although REAN tends to miss the lowest CO mixing ratios for the four seasons and tends to oversample the extra-tropical transition layer (ExTL region) in spring. This evaluation stresses the importance of the model gradients for a good description of the mixing in the Ex-UTLS region, which is inherently difficult to observe from satellite instruments.

The first regular measurements of ozone, carbon monoxide and water vapour in the Pacific UTLS by IAGOS

We present the features seen in the first 2 months (July and August 2012) of data collected over the Pacific by IAGOS (In-service Aircraft for a Global Observing System)-equipped aircraft. IAGOS is the continuation and development of the well-known MOZAIC (Measurement of Ozone and Water Vapour on Airbus in-service Aircraft) project where scientific instruments were carried on commercially operated A340 aircraft to make measurements of chemical species in the atmosphere. Here, we show data from an aircraft operated by China Airlines on routes from Taipei to Vancouver, which provided the first trans-Pacific measurements by an IAGOS-equipped aircraft. We describe the chemical composition of the extratropical upper troposphere/lower stratosphere (Ex-UTLS) across the Pacific basin in the Northern Hemisphere. The observed concentrations of ozone span a range from 18 to 500 ppbv indicating sources in the marine boundary layer and lowermost stratosphere, respectively. Concentrations of carbon monoxide (CO) greater than 400 ppbv are observed in the Ex-UTLS suggesting that plumes of pollution have been exported from the continent. These low concentrations of ozone and high concentrations of CO were rarely recorded in 8 yr of MOZAIC observations over the Atlantic.