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Atmospheric Measurement Techniques An interactive open-access journal of the European Geosciences Union
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Volume 7, issue 5
Atmos. Meas. Tech., 7, 1385–1394, 2014
© Author(s) 2014. This work is distributed under
the Creative Commons Attribution 3.0 License.
Atmos. Meas. Tech., 7, 1385–1394, 2014
© Author(s) 2014. This work is distributed under
the Creative Commons Attribution 3.0 License.

Research article 21 May 2014

Research article | 21 May 2014

DIAL measurement of lower tropospheric ozone over Saga (33.24° N, 130.29° E), Japan, and comparison with a chemistry–climate model

O. Uchino1,2, T. Sakai2, T. Nagai2, I. Morino1, T. Maki2, M. Deushi2, K. Shibata2, M. Kajino2, T. Kawasaki3, T. Akaho3, S. Takubo3, H. Okumura3, K. Arai3, M. Nakazato4, T. Matsunaga1, T. Yokota1, S. Kawakami5, K. Kita6, and Y. Sasano1 O. Uchino et al.
  • 1National Institute for Environmental Studies, 16-2 Onogawa, Tsukuba, Ibaraki 305-8506, Japan
  • 2Meteorological Research Institute, 1-1 Nagamine, Tsukuba, Ibaraki 305-0052, Japan
  • 3Saga University, 1 Honjou, Saga, Saga 840-8502, Japan
  • 4Japan Meteorological Agency, 1-3-4 Otemachi, Chiyoda-ku, Tokyo 100-8122, Japan
  • 5Japan Aerospace Exploration Agency, 2-1-1 Sengen, Tsukuba, Ibaraki 305-8505, Japan
  • 6Ibaraki University, 2-1-1 Bunkyo, Mito, Ibaraki 310-8512, Japan

Abstract. We have improved an ozone DIfferential Absorption Lidar (DIAL) system, originally developed in March 2010. The improved DIAL system consists of a Nd:YAG laser and a 2 m Raman cell filled with 8.1 × 105 Pa of CO2 gas which generate four Stokes lines (276, 287, 299, and 312 nm) of stimulated Raman scattering, and two receiving telescopes with diameters of 49 and 10 cm. Using this system, 44 ozone profiles were observed in the 1–6 km altitude range over Saga (33.24° N, 130.29° E) in 2012. High-ozone layers were observed at around 2 km altitude during April and May. Ozone column amounts within the 1–6 km altitude range were almost constant (19.1 DU on average) from January to March, and increased to 26.7 DU from late April to July. From mid-July through August, ozone column amounts decreased greatly to 14.3 DU because of exchanges of continental and maritime air masses. Then in mid-September they increased again to 22.1 DU within 1−6 km, and subsequently decreased slowly to 17.3 DU, becoming almost constant by December.

The Meteorological Research Institute's chemistry–climate model version 2 (MRI-CCM2) successfully predicted most of these ozone variations with the following exceptions. MRI-CCM2 could not predict the high-ozone volume mixing ratios measured at around 2 km altitude on 5 May and 11 May, possibly in part because emissions were assumed in the model to be constant (climatological data were used). Ozone volume mixing ratios predicted by MRI-CCM2 were low in the 2–6 km range on 7 July and high in the 1–4 km range on 19 July compared with those measured by DIAL.

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