Jan-bai Nee

Dr. Jan-bai Nee


Research Focus & Metrics

Academic Career Length

37Years (1990-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
21 June 2011 in Journal of Geophysical Research
Verified
Journal Article
Closed access
PDF file
SDSubrata Kumar Das
Subrata Kumar Das
CCChih-Wei Chiang
Chih-Wei Chiang
JNJan-bai Nee
Jan-bai Nee

25 June 2018 in Remote Sensing
Verified
Journal Article
Open access
PDF file
Zhongwei HuangZhongwei Huang
Zhongwei Huang
JNJan-bai Nee
Jan-bai Nee
CCChih-Wei Chiang
Chih-Wei Chiang
Shuang ZhangShuang Zhang
Shuang Zhang
HJHongchun Jin
Hongchun Jin
TZTian Zhou
Tian Zhou
Dust aerosols have significant impact on the environment and climate through long-range transport. We report, in this paper, a case of dust–cloud interaction process using combined measurements of a ground-based polarization and Raman (PR) lidar systems, and implemented by the spaceborne Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observations (CALIPSO) lidar observations. The dust event occurred on 14 March 2009 over East Asia. During the two hours of observing time, the ground-based lidar observed an ongoing process of decreasing of the depolarization ratio (DR) accompanied by the increase of the water vapor simultaneously, indicating a dust–cloud interaction and particle transformation. CALIPSO measurements also found similar layers of dusts and clouds over lands and oceans with properties similar to the ground based lidar measurements. Our observation was a real-time dust–cloud process with the observation of occurrence of particle transformation. The depolarization reduced from 0.2 to 0.1 corresponding to a change of aspect ratio from 1.2 to 1.1. A discussion of a dust–cloud interaction in terms of three-stage cloud processes is made based on back-trajectory analyses and lidar observations. The result shows that dust aerosols decrease the cloud extinction coefficient by 41% but increase the cloud optical depth (COD) of water cloud by 12.79%, compared with that of pure water clouds. Furthermore, if dust aerosols participate as cloud condensation nuclei (CCN) in cloud physical processes, then they significantly reduce the size of the cloud droplet by 44–79%. Finally, based on three-year collocated CALIPSO and CloudSat measurements from 2007 to 2010, we found approximately one-third of clouds are originally dusty in the spring over the Pacific Coast areas.

3 August 2007 in Journal of Geophysical Research: Atmospheres
Verified
Journal Article
Closed access
PDF file
JNJan-bai Nee
Jan-bai Nee
CCChih‐Wei Chiang
Chih‐Wei Chiang
HHHuan‐Ling Hu
Huan‐Ling Hu
SHShun‐Xing Hu
Shun‐Xing Hu
Jia-Yuh YuJia-Yuh Yu
Jia-Yuh Yu

26 October 2007 in Journal of Quantitative Spectroscopy and Radiative Transfer
Verified
Journal Article
Closed access
CCChih-Wei Chiang
Chih-Wei Chiang
SDSubrata Kumar Das
Subrata Kumar Das
JNJan-bai Nee
Jan-bai Nee

19 April 2012 in Annales Geophysicae
Verified
Journal Article
Open access
PDF file
HGH. Gao
H. Gao
JNJan-bai Nee
Jan-bai Nee
JXJ. Xu
J. Xu
Emissions of the 557.7 nm green line airglow observed by the ISUAL (Imager of Sprites and Upper Atmospheric Lightning) instrument on board the FORMOSAT-2 satellite in May and November 2008 are studied here to derive the density distributions of the atomic oxygen by using atmospheric parameters from MSISE-00 model and TIMED (Thermosphere Ionosphere Mesosphere Energetics and Dynamics)/SABER (Sounding of the Atmosphere using Broadband Emission Radiometry) measurements. The May observations were made in 10 days from a fixed orbit of longitude (100° E) with the results showing emission rate and O atom density both peaked at heights of about 90 km over 10° to 20° latitudes in the Northern Hemisphere (NH). In the Southern Hemisphere (SH), the emission rate and density of O atom are both low compared with those in NH. In November, the observations were made as the satellite traveled over all 14 orbits around the earth, covering all longitudes and latitudes of 25° S–45° N. Strong peaks of emission rates and O atoms are found at heights of about 95 km in the mid-latitudes in both hemispheres. In the equator, the airglow layer has a weaker emission rate but with higher altitude compared with those of mid-latitudes. In the lower and upper mesosphere at heights below 85 km and above 105 km, there are more O atoms in the equatorial regions than in the mid-latitudes. And there is a good correlation between the O atom and the temperature structure. A comparison with O atom distribution derived from OH airglow observed by TIMED/SABER at about the same time shows similar results.

20 August 1990 in Journal of Geophysical Research: Atmospheres
Verified
Journal Article
Closed access
PDF file
JSJames Schwab
James Schwab
EWE. M. Weinstock
E. M. Weinstock
JNJan-bai Nee
Jan-bai Nee
JAJ. G. Anderson
J. G. Anderson