We developed an automated compact mobile Raman lidar (MRL) system for measuring the vertical distribution of the water vapor mixing ratio (w) in the lower troposphere, which has an affordable cost and is easy to operate. The MRL was installed in a small trailer for easy deployment and can start measurement in a few hours, and it is capable of unattended operation for several months. We describe the MRL system and present validation results obtained by comparing the MRL-measured data with collocated radiosonde, Global Navigation Satellite System (GNSS), and high-resolution objective analysis data. The comparison results showed that MRL-derived w agreed within 10 % (rootmean-square difference of 1.05 g kg −1 ) with values obtained by radiosonde at altitude ranges between 0.14 and 1.5 km in the daytime and between 0.14 and 5-6 km at night in the absence of low clouds; the vertical resolution of the MRL measurements was 75-150 m, their temporal resolution was less than 20 min, and the measurement uncertainty was less than 30 %. MRL-derived precipitable water vapor values were similar to or slightly lower than those obtained by GNSS at night, when the maximum height of MRL measurements exceeded 5 km. The MRL-derived w values were at most 1 g kg −1 (25 %) larger than local analysis data. A total of 4 months of continuous operation of the MRL system demonstrated its utility for monitoring water vapor distributions in the lower troposphere.Published by Copernicus Publications on behalf of the European Geosciences Union.

Abstract:The Total Carbon Column Observing Network (TCCON) is a global network dedicated to the precise and accurate measurements of greenhouse gases (GHG) in the atmosphere. The TCCON station in Burgos, Ilocos Norte, Philippines was established with the primary purpose of validating the upcoming Greenhouse gases Observing SATellite-2 (GOSAT-2) mission and in general, to respond to the need for reliable ground-based validation data for satellite GHG observations in the region. Here, we present the first 4 months of data from the new TCCON site in Burgos, initial comparisons with satellite measurements of CO 2 and model simulations of CO. A nearest sounding from Japan's GOSAT as well as target mode observations from NASA's Orbiting Carbon Observatory 2 (OCO-2) showed very good consistency in the retrieved column-averaged dry air mole fractions of CO 2 , yielding TCCON -satellite differences of 0.86 ± 1.06 ppm for GOSAT and 0.83 ± 1.22 ppm for OCO-2. We also show measurements of enhanced CO, probably from East Asia. GEOS-Chem model simulations were used to study the observed CO variability. However, despite the model capturing the pattern of the CO variability, there is an obvious underestimation in the CO magnitude in the model. We conclude that more measurements and modeling are necessary to adequately sample the variability over different seasons and to determine the suitability of current inventories.

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Abstract. To validate products of the Greenhouse gases Observing SATellite (GOSAT), we observed vertical profiles of aerosols, thin cirrus clouds, and tropospheric ozone with a mobile-lidar system that consisted of a two-wavelength (532 and 1064 nm) polarization lidar and a tropospheric ozone differential absorption lidar (DIAL). We used these lidars to make continuous measurements over Saga (33.24 • N, 130.29 • E) during 20-31 March 2015. High ozone and high aerosol concentrations were observed almost simultaneously in the altitude range 0.5-1.5 km from 03:00 to 20:00 Japan Standard Time (JST) on 22 March 2015. The maximum ozone volume mixing ratio was ∼ 110 ppbv. The maxima of the aerosol extinction coefficient and optical depth at 532 nm were 1.2 km −1 and 2.1, respectively. Backward trajectory analysis and the simulations by the Model of Aerosol Species IN the Global AtmospheRe (MASINGAR) mk-2 and the Meteorological Research Institute Chemistry-Climate Model, version 2 (MRI-CCM2), indicated that mineral dust particles from the Gobi Desert and an air mass with high ozone and aerosol (mainly sulfate) concentrations that originated from the North China Plain could have been transported over the measurement site within about 2 days. These high ozone and aerosol concentrations impacted surface air quality substantially in the afternoon of 22 March 2015. After some modifications of its physical and chemical parameters, MRI-CCM2 approximately reproduced the high ozone volume mixing ratio. MASINGAR mk-2 successfully predicted high aerosol concentrations, but the predicted peak aerosol optical thickness was about one-third of the observed value.

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