The nationwide lockdown due to the COVID-19 pandemic in 2020 reduced industrial and human activities in China. In this study, we investigate atmospheric carbon monoxide (CO) concentration changes ...during the lockdown from observations at the surface and from two satellites (TROPOspheric Monitoring Instrument (TROPOMI) and Infrared Atmospheric Sounding Interferometer (IASI)). It is found that the average CO surface concentration in 2020 was close to that in 2019 before the lockdown, and became 18.7% lower as compared to 2019 during the lockdown. The spatial variation of the change in the CO surface concentration is high, with an 8–27% reduction observed for Beijing, Shanghai, Chengdu, Zhengzhou, and Guangzhou, and almost no change in Wuhan. The TROPOMI and IASI satellite observations show that the CO columns decreased by 2–13% during the lockdown in most regions in China. However in South China, there was an 8.8% increase in the CO columns observed by TROPOMI and a 36.7% increase observed by IASI, which is contrary to the 23% decrease in the surface CO concentration. The enhancement of the CO column in South China is strongly affected by the fire emissions transported from Southeast Asia. This study provides an insight into the impact of COVID-19 on CO concentrations both at the surface and in the columns in China, and it can be extended to evaluate other areas using the same approach.
Robust calibration and validation (Cal and Val) should guarantee the accuracy of the retrieved information, make the remote sensing data consistent and traceable, and maintain the sensor performance ...during the operational phase. The DRAGON program has set up many remote sensing research topics on various application domains. In order to promote the effectiveness of data modeling and interpretation, it is necessary to solve various challenges in Cal and Val for quantitative RS applications. This project in the DRAGON 4 program aims to promote the cooperation of the Cal and Val experts from European and Chinese institutes in Cal and Val activities, and several achievements have been obtained in the advanced on-orbit optical sensor calibration, as well as microwave remote sensor calibration and product generation. The outcomes of the project have benefited the related remote sensing modeling and product retrieval, and promoted the radiometric calibration network (RadCalNet) as an international operational network for calibration, intercalibration, and validation. Moreover, this project provided local governments with a more accurate OMI NO2 data in China, which were used to study the air quality control during APEC period, Parade period and G20 period. This will be of ongoing be value for monitoring atmospheric environmental quality and formulating pollution control strategies.
The thermal And near infrared sensor for carbon observations Fourier transform spectrometer (TANSO-FTS) on board the Greenhouse Gases Observing Satellite (GOSAT) applies the normal nadir mode above ...the land (“land data”) and sun glint mode over the ocean (“ocean data”) to provide global distributions of column-averaged dry-air mole fractions of CO2 and CH4, or XCO2 and XCH4. Several algorithms have been developed to obtain highly accurate greenhouse gas concentrations from TANSO-FTS/GOSAT spectra. So far, all the retrieval algorithms have been validated with the measurements from ground-based Fourier transform spectrometers from the Total Carbon Column Observing Network (TCCON), but limited to the land data. In this paper, the ocean data of the SRPR, SRFP (the proxy and full-physics versions 2.3.5 of SRON/KIT's RemoTeC algorithm), NIES (National Institute for Environmental Studies operational algorithm version 02.21) and ACOS (NASA's Atmospheric CO2 Observations from Space version 3.5) are compared with FTIR measurements from five TCCON sites and nearby GOSAT land data.For XCO2, both land and ocean data of NIES, SRFP and ACOS show good agreement with TCCON measurements. Averaged over all TCCON sites, the relative biases of ocean data and land data are −0.33 and −0.13 % for NIES, 0.03 and 0.04 % for SRFP, 0.06 and −0.03 % for ACOS, respectively. The relative scatter ranges between 0.31 and 0.49 %. For XCH4, the relative bias of ocean data is even less than that of the land data for the NIES (0.02 vs. −0.35 %), SRFP (0.04 vs. 0.20 %) and SRPR (−0.02 vs. 0.06 %) algorithms. Compared to the results for XCO2, the XCH4 retrievals show larger relative scatter (0.65–0.81 %).
Sulphur dioxide (SO2 ) fluxes of active degassing volcanoes are routinely measured with ground-based equipment to characterize and monitor volcanic activity. SO2 of unmonitored volcanoes or from ...explosive volcanic eruptions, can be measured with satellites. However, remote-sensing methods based on absorption spectroscopy generally provide integrated amounts of already dispersed plumes of SO2 and satellite derived flux estimates are rarely reported. Here we review a number of different techniques to derive volcanic SO2 fluxes using satellite measurements of plumes of SO2 and investigate the temporal evolution of the total emissions of SO2 for three very different volcanic events in 2011: Puyehue-Cordón Caulle (Chile), Nyamulagira (DR Congo) and Nabro (Eritrea). High spectral resolution satellite instruments operating both in the ultraviolet-visible (OMI/Aura and GOME-2/MetOp-A) and thermal infrared (IASI/MetOp-A) spectral ranges, and multispectral satellite instruments operating in the thermal infrared (MODIS/Terra-Aqua) are used. We show that satellite data can provide fluxes with a sampling of a day or less (few hours in the best case). Generally the flux results from the different methods are consistent, and we discuss the advantages and weaknesses of each technique. Although the primary objective of this study is the calculation of SO2 fluxes, it also enables us to assess the consistency of the SO2 products from the different sensors used.
Carbon monoxide (CO), acetylene (C.sub.2 H.sub.2 ), ethane (C.sub.2 H.sub.6 ), formaldehyde (H.sub.2 CO), and hydrogen cyanide (HCN) are important trace gases in the atmosphere. They are highly ...related to biomass burning, fossil fuel combustion, and biogenic emissions globally, affecting air quality and climate change. However, the variations and correlations among these species are not well known in northern China due to limited measurements. In June 2018, we installed a new ground-based Fourier transform infrared (FTIR) spectrometer (Bruker IFS 125HR) recording mid-infrared high spectral resolution solar-absorption spectra at Xianghe (39.75.sup." N, 116.96.sup." E), China. In this study, we use the latest SFIT4 code, together with advanced a priori profiling and spectroscopy, to retrieve these five species from the FTIR spectra measured between June 2018 and November 2021. The retrieval strategies, retrieval information and retrieval uncertainties are presented and discussed. For the first time, the time series, variations, and correlations of these five species are analyzed at a typical polluted site in northern China. The seasonal variations in C.sub.2 H.sub.2 and C.sub.2 H.sub.6 total columns show a maximum in winter-spring and a minimum in autumn, whereas the seasonal variations in H.sub.2 CO and HCN show a maximum in summer and a minimum in winter. Unlike the other four species, the FTIR measurements show that there is almost no seasonal variation in the CO column. The correlation coefficients (R) between the synoptic variations in CO and the other four species (C.sub.2 H.sub.2, C.sub.2 H.sub.6, H.sub.2 CO, and HCN) are between 0.68 and 0.80, indicating that they are affected by common sources. Using the FLEXPART model backward simulations and satellite fire measurements, we find that the variations in CO, C.sub.2 H.sub.2, C.sub.2 H.sub.6, and H.sub.2 CO columns are mainly dominated by the local anthropogenic emissions, while HCN column observed at Xianghe is a good tracer to identify fire emissions.
Carbon monoxide (CO), acetylene (C2H2), ethane (C2H6), formaldehyde (H2CO), and hydrogen cyanide (HCN) are important trace gases in the atmosphere. They are highly related to biomass burning, fossil ...fuel combustion, and biogenic emissions globally, affecting air quality and climate change. However, the variations and correlations among these species are not well known in northern China due to limited measurements. In June 2018, we installed a new ground-based Fourier transform infrared (FTIR) spectrometer (Bruker IFS 125HR) recording mid-infrared high spectral resolution solar-absorption spectra at Xianghe (39.75∘ N, 116.96∘ E), China. In this study, we use the latest SFIT4 code, together with advanced a priori profiling and spectroscopy, to retrieve these five species from the FTIR spectra measured between June 2018 and November 2021. The retrieval strategies, retrieval information and retrieval uncertainties are presented and discussed. For the first time, the time series, variations, and correlations of these five species are analyzed at a typical polluted site in northern China. The seasonal variations in C2H2 and C2H6 total columns show a maximum in winter–spring and a minimum in autumn, whereas the seasonal variations in H2CO and HCN show a maximum in summer and a minimum in winter. Unlike the other four species, the FTIR measurements show that there is almost no seasonal variation in the CO column. The correlation coefficients (R) between the synoptic variations in CO and the other four species (C2H2, C2H6, H2CO, and HCN) are between 0.68 and 0.80, indicating that they are affected by common sources. Using the FLEXPART model backward simulations and satellite fire measurements, we find that the variations in CO, C2H2, C2H6, and H2CO columns are mainly dominated by the local anthropogenic emissions, while HCN column observed at Xianghe is a good tracer to identify fire emissions.
Carbon monoxide (CO), acetylene (C2H2), ethane (C2H6), formaldehyde (H2CO), and hydrogen cyanide (HCN) are important trace gases in the atmosphere. They are highly related to biomass burning, fossil ...fuel combustion, and biogenic emissions globally, affecting air quality and climate change. However, the variations and correlations among these species are not well known in northern China due to limited measurements. In June 2018, we installed a new ground-based Fourier transform infrared (FTIR) spectrometer (Bruker IFS 125HR) recording mid-infrared high spectral resolution solar-absorption spectra at Xianghe (39.75∘ N, 116.96∘ E), China. In this study, we use the latest SFIT4 code, together with advanced a priori profiling and spectroscopy, to retrieve these five species from the FTIR spectra measured between June 2018 and November 2021. The retrieval strategies, retrieval information and retrieval uncertainties are presented and discussed. For the first time, the time series, variations, and correlations of these five species are analyzed at a typical polluted site in northern China. The seasonal variations in C2H2 and C2H6 total columns show a maximum in winter–spring and a minimum in autumn, whereas the seasonal variations in H2CO and HCN show a maximum in summer and a minimum in winter. Unlike the other four species, the FTIR measurements show that there is almost no seasonal variation in the CO column. The correlation coefficients (R) between the synoptic variations in CO and the other four species (C2H2, C2H6, H2CO, and HCN) are between 0.68 and 0.80, indicating that they are affected by common sources. Using the FLEXPART model backward simulations and satellite fire measurements, we find that the variations in CO, C2H2, C2H6, and H2CO columns are mainly dominated by the local anthropogenic emissions, while HCN column observed at Xianghe is a good tracer to identify fire emissions.
Nitric oxide (NO) is a key active trace gas in the atmosphere, which contributes to form harmful ozone in the troposphere and to the destruction of ozone in the stratosphere. In this study, we ...present the NO retrieval from ground-based Fourier-transform infrared (FTIR) solar absorption spectrometry measurements at a polluted site (Xianghe, China) and a background site (Maïdo, Reunion Island). The degree of freedom (DOF) of the NO retrieval is 2.3±0.4 (1Ï) at Xianghe and 1.3±0.1 at Maïdo.
Isentropic mixing properties in the stratosphere modeled by the forward calculation of an inverse model (TM5‐4DVAR) are evaluated against Michelson Interferometer for Passive Atmospheric Sounding ...(MIPAS) and Microwave Limb Sounder (MLS) observations. The isentropic mixing processes are separated into large‐scale stirring described by the “equivalent length” and small‐scale diffusion described by the diffusivity. Compared to the measurements, we find that the modeled stirring is not strong enough and that the small‐scale diffusivity is too large. TM5‐4DVAR produces excessive mixing‐induced poleward flux for stratospheric CH4. The flux convergence presents negative biases in the tropics and positive biases in the polar regions. The biases cannot be reduced by improving the horizontal resolution only. Modeled isentropic mixing depends on the horizontal as well as the vertical resolution of the model. An increase in vertical resolution reduces numerical diffusion of the model in the vertical. The decreased vertical diffusion leads to reduction in the modeled isentropic diffusivity. Biases in modeled total column‐averaged mixing ratios of CH4 are significant for both models with a coarse vertical resolution of 4° × 6° × 25 (and 2° × 3° × 25, 1° × 1° × 25) and an improved one of 1° × 1° × 40. They are estimated to be 7–14 and 3–7 ppb in the winter extratropics under the assumption that isentropic mixing is dominant over vertical transport on a time scale of 3 days. Correspondingly, resulted biases in inverted CH4 surface emissions are estimated to be 0.5–1 and 0.2–0.5 mg/m2/hr, respectively, in the extratropics.
Key Points
A significant improvement in the modeled isentropic mixing in the stratosphere is obtained if the vertical resolution is improved there
The thermal And near infrared sensor for carbon observations Fourier transform spectrometer (TANSO-FTS) on board the Greenhouse Gases Observing Satellite (GOSAT) applies the normal nadir mode above ...the land ("land data") and sun glint mode over the ocean ("ocean data") to provide global distributions of column-averaged dry-air mole fractions of CO2 and CH4, or XCO2 and XCH4. Several algorithms have been developed to obtain highly accurate greenhouse gas concentrations from TANSO-FTS/GOSAT spectra. So far, all the retrieval algorithms have been validated with the measurements from ground-based Fourier transform spectrometers from the Total Carbon Column Observing Network (TCCON), but limited to the land data. In this paper, the ocean data of the SRPR, SRFP (the proxy and full-physics versions 2.3.5 of SRON/KIT's RemoTeC algorithm), NIES (National Institute for Environmental Studies operational algorithm version 02.21) and ACOS (NASA's Atmospheric CO2 Observations from Space version 3.5) are compared with FTIR measurements from five TCCON sites and nearby GOSAT land data.
For XCO2, both land and ocean data of NIES, SRFP and ACOS show good agreement with TCCON measurements. Averaged over all TCCON sites, the relative biases of ocean data and land data are -0.33 and -0.13-% for NIES, 0.03 and 0.04-% for SRFP, 0.06 and -0.03-% for ACOS, respectively. The relative scatter ranges between 0.31 and 0.49-%. For XCH4, the relative bias of ocean data is even less than that of the land data for the NIES (0.02 vs. -0.35-%), SRFP (0.04 vs. 0.20-%) and SRPR (-0.02 vs. 0.06-%) algorithms. Compared to the results for XCO2, the XCH4 retrievals show larger relative scatter (0.65-0.81-%).
PDF
