Zhaonan Cai

Prof. Dr. Zhaonan Cai


Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

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

Representative Publications

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13 November 2019 in Light: Science & Applications
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Journal Article
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Chengxin ZhangChengxin Zhang
Chengxin Zhang
WTWei Tan
Wei Tan
QHQihou Hu
Qihou Hu
ZCZhaonan Cai
Zhaonan Cai
WSWenjing Su
Wenjing Su
Jianguo LiuJianguo Liu
Jianguo Liu
Abundances of a range of air pollutants can be inferred from satellite UV-Vis spectroscopy measurements by using the unique absorption signatures of gas species. Here, we implemented several spectral fitting methods to retrieve tropospheric NO2, SO2, and HCHO from the ozone monitoring instrument (OMI), with radiative simulations providing necessary information on the interactions of scattered solar light within the atmosphere. We analyzed the spatial distribution and temporal trends of satellite-observed air pollutants over eastern China during 2005–2017, especially in heavily polluted regions. We found significant decreasing trends in NO2 and SO2 since 2011 over most regions, despite varying temporal features and turning points. In contrast, an overall increasing trend was identified for tropospheric HCHO over these regions in recent years. Furthermore, generalized additive models were implemented to understand the driving forces of air quality trends in China and assess the effectiveness of emission controls. Our results indicated that although meteorological parameters, such as wind, water vapor, solar radiation and temperature, mainly dominated the day-to-day and seasonal fluctuations in air pollutants, anthropogenic emissions played a unique role in the long-term variation in the ambient concentrations of NO2, SO2, and HCHO in the past 13 years. Generally, recent declines in NO2 and SO2 could be attributed to emission reductions due to effective air quality policies, and the opposite trends in HCHO may urge the need to control anthropogenic volatile organic compound (VOC) emissions.

1 April 2021 in Science of The Total Environment
Verified
Journal Article
Closed access
FZFei Zhao
Fei Zhao
WTWei Tan
Wei Tan
ZCZhaonan Cai
Zhaonan Cai
XLXiong Liu
Xiong Liu
JBJuseon Bak
Juseon Bak
JLJianguo Liu
Jianguo Liu

16 June 2022 in Environmental Research Letters
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Journal Article
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KCKe Che
Ke Che
ZCZhaonan Cai
Zhaonan Cai
YLYi Liu
Yi Liu
LWLin Wu
Lin Wu
DYDongxu Yang
Dongxu Yang
PWPucai Wang
Pucai Wang
We estimated CO2 emissions from the Beijing region of China using differential ground-based observations of the column-averaged dry air mole fractions of CO2 ( Δ X C O 2 ,  obs ; urban minus upwind background column observations) in winter (1 November 2020–1 March 2021). Beijing is one of the most world’s populated cities and the CO2 emissions from this region contain large uncertainties in different bottom-up anthropogenic inventories. Differential measurements are potentially able to capture urban signals over Beijing (3.46 ± 2.35 ppm). The simulated XCO2 enhancements were calculated ( Δ X C O 2 ,  sim ) based on three emission inventories (the Open-source Data Inventory for Anthropogenic CO2 (ODIAC), Multiresolution Emission Inventory for China (MEIC) and Emissions Database for Global Atmospheric Research (EDGAR) datasets) for Beijing. The Δ X C O 2 ,  sim values based on the ODIAC dataset were much higher than the observations, whereas the values from the EDGAR dataset were much lower and the MEIC dataset was more consistent. We performed a Lagrangian inversion framework based on Bayesian theory. The average and uncertainty of a priori estimates (12.18 ± 8.0, 7.09 ± 7.5 and 3.53 ± 11.4 μmol (m2 s)−1) were optimized to the posterior emissions (9.44 ± 5.7, 7.13 ± 4.9 and 7.15 ± 5.7 μmol (m2 s)−1), suggesting that the three posterior estimates tended to converge to become more consistent, transport errors (especially the horizontal transport errors) and the spatially uneven corrections in Beijing were the main reason for the differences between the posterior estimates. Sensitivity tests suggested that the prescribed spatial and temporal structures affected up to about 12.9%, 4.9% and 20.8%, respectively, of the three inventories.

11 May 2022 in Advances in Atmospheric Sciences
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Journal Article
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KCKe Che
Ke Che
YLYi Liu
Yi Liu
ZCZhaonan Cai
Zhaonan Cai
DYDongxu Yang
Dongxu Yang
HWHaibo Wang
Haibo Wang
PWPucai Wang
Pucai Wang

5 August 2022 in Remote Sensing
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MZMinqiang Zhou
Minqiang Zhou
QNQichen Ni
Qichen Ni
ZCZhaonan Cai
Zhaonan Cai
BLBavo Langerock
Bavo Langerock
WNWeidong Nan
Weidong Nan
PWPucai Wang
Pucai Wang
Monitoring the atmospheric CO2 columns inside and around a city is of great importance to understand the temporal–spatial variation of XCO2 near strong anthropogenic emissions. In this study, we use two FTIR CO2 column measurements in Beijing (Bruker EM27/SUN) and Xianghe (Bruker IFS 125HR) between 2019 and 2021 to investigate the differences of XCO2 between Beijing (urban) and Xianghe (suburb) in North China and to validate the OCO-2 and OCO-3 satellite XCO2 retrievals. The mean and standard deviation (std) of the ΔXCO2 between Beijing and Xianghe (Beijing–Xianghe) observed by two FTIR instruments are 0.206 ± 1.736 ppm, which has a seasonal variation and varies with meteorological conditions (wind speed and wind direction). The mean and std of the XCO2 differences between co-located satellite and FTIR measurements are −0.216 ± 1.578 ppm in Beijing and −0.343 ± 1.438 ppm in Xianghe for OCO-2 and 0.637 ± 1.594 ppm in Beijing and 1.206 ± 1.420 ppm in Xianghe for OCO-3. It is found that the OCO-3 snapshot area mode (SAM) measurements can capture the spatial gradient of XCO2 between urban and suburbs well. However, the FTIR measurements indicate that the OCO-3 SAM measurements are about 0.9–1.4 ppm overestimated in Beijing and Xianghe.

8 July 2021 in Remote Sensing
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Journal Article
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HBHartmut Boesch
Hartmut Boesch
YLYi Liu
Yi Liu
JTJohanna Tamminen
Johanna Tamminen
DYDongxu Yang
Dongxu Yang
TPThe University of Edinburgh Palmer
The University of Edinburgh Palmer
HCHuilin Chen
Huilin Chen
The increase in atmospheric greenhouse gas concentrations of CO2 and CH4, due to human activities, is the main driver of the observed increase in surface temperature by more than 1 °C since the pre-industrial era. At the 2015 United Nations Climate Change Conference held in Paris, most nations agreed to reduce greenhouse gas emissions to limit the increase in global surface temperature to 1.5 °C. Satellite remote sensing of CO2 and CH4 is now well established thanks to missions such as NASA’s OCO-2 and the Japanese GOSAT missions, which have allowed us to build a long-term record of atmospheric GHG concentrations from space. They also give us a first glimpse into CO2 and CH4 enhancements related to anthropogenic emission, which helps to pave the way towards the future missions aimed at a Monitoring & Verification Support (MVS) capacity for the global stock take of the Paris agreement. China plays an important role for the global carbon budget as the largest source of anthropogenic carbon emissions but also as a region of increased carbon sequestration as a result of several reforestation projects. Over the last 10 years, a series of projects on mitigation of carbon emission has been started in China, including the development of the first Chinese greenhouse gas monitoring satellite mission, TanSat, which was successfully launched on 22 December 2016. Here, we summarise the results of a collaborative project between European and Chinese teams under the framework of the Dragon-4 programme of ESA and the Ministry of Science and Technology (MOST) to characterize and evaluate the datasets from the TanSat mission by retrieval intercomparisons and ground-based validation and to apply model comparisons and surface flux inversion methods to TanSat and other CO2 missions, with a focus on China.