Ground-based Multi-axis Differential Optical Absorption Spectroscopy Research Articles

Retrieval of Tropospheric NO2 Vertical Column Densities from Ground-Based MAX-DOAS Measurements in Lhasa, a City on the Tibetan Plateau

In order to investigate the abundance of and temporal variation in nitrogen dioxide (NO2) in the troposphere and validate the corresponding satellite products during a normal year and the lockdown period of coronavirus disease 2019 (COVID-19) in Lhasa, a city on the Tibetan Plateau (TP), ground-based remote-sensing measurements captured by applying multi-axis differential optical absorption spectroscopy (MAX-DOAS) were recorded from August 2021 to March 2023 at the Lhasa site (91.14°E, 29.66°N; 3552.5 m altitude). The NO2 differential slant column densities (dSCDs) were retrieved from the spectra of scattered solar light at different elevation angles. Then, the tropospheric NO2 vertical column densities (VCDs) were calculated with the geometric approximation method. Based on the retrieved tropospheric NO2 VCDs, we found that the pattern of monthly variation in tropospheric NO2 VCDs in Lhasa presented two peaks, one in winter and one around May. According to the monthly means of tropospheric NO2 VCDs during the COVID-19 lockdown, the NO2 background level in Lhasa was estimated to be 0.53 × 1015 molecules·cm−2. For diurnal variations in tropospheric NO2 VCDs, the morning and evening peaks disappeared during the COVID-19 lockdown period. The east–west direction (i.e., along the river valley) was the main path of NO2 transport and dispersion in Lhasa, but the tropospheric NO2 VCDs were little dependent on the wind direction or wind speed during the COVID-19 lockdown. The correlation coefficient of tropospheric NO2 VCDs was R = 0.33 (R = 0.43), with the averaged relative deviation of −28% (99%) for the TROPOMI (GEMS) relative to ground-based MAX-DOAS. The monthly deviations of tropospheric NO2 VCDs between ground-based MAX-DOAS and the satellite showed a dependence on NO2 abundance, with the maxima of the monthly positive deviations during the COVID-19 lockdown period. The GEMS could not capture the strong and systematic diurnal variation in tropospheric NO2 VCDs in the “normal” year well. During the COVID-19 lockdown, the GEMS (>2 × 1015 molecules·cm−2) overestimated the hourly levels measured by ground-based MAX-DOAS (<1.6 × 1015 molecules·cm−2). As a whole, these results are beneficial to understanding the influences of anthropogenic activities on NO2 background levels in Lhasa and to learning the accuracy of satellite products over the TP, with its high altitude and complex terrain.

Horizontal distribution of tropospheric NO2 and aerosols derived by dual-scan multi-wavelength multi-axis differential optical absorption spectroscopy (MAX-DOAS) measurements in Uccle, Belgium

Abstract. Dual-scan ground-based multi-axis differential optical absorption spectroscopy (MAX-DOAS) measurements of tropospheric nitrogen dioxide (NO2) and aerosols were carried out in Uccle (50.8∘ N, 4.35∘ E; Brussels region, Belgium) for 2 years from March 2018 to February 2020. The MAX-DOAS instrument operated in both UV and visible wavelength ranges in a dual-scan configuration consisting of two submodes: (1) an elevation scan in a fixed viewing azimuthal direction and (2) an azimuthal scan in a fixed low elevation angle (2∘). By analyzing the O4 and NO2 differential slant column density (dSCD) at six different wavelength intervals along every azimuthal direction and by applying a new optimal-estimation-based inversion approach (the so-called mapping MAX-DOAS technique), the horizontal distribution of the NO2 near-surface concentrations and vertical column densities (VCDs) as well as the aerosol near-surface extinction coefficients are retrieved along 10 azimuthal directions. The retrieved horizontal NO2 concentration profiles allow the identification of the main NO2 hotspots in the Brussels area. Correlative comparisons of the retrieved horizontal NO2 distribution were conducted with airborne, mobile, air quality model, and satellite datasets, and overall good agreement is found. The comparison with TROPOMI observations from operational and scientific data products reveals that the characterization of the horizontal distribution of tropospheric NO2 VCDs by ground-based measurements and an adequate a priori NO2 profile shape in TROPOMI retrievals lead to better consistency between satellite and ground-based datasets.

Ground-Based MAX-DOAS Measurements of Tropospheric Aerosols, NO2, and HCHO Distributions in the Urban Environment of Shanghai, China

Aerosol extinction profiles at 550 nm were retrieved by applying multi-axis differential optical absorption spectroscopy (MAX-DOAS) and lookup table. Then the tropospheric NO2 and HCHO vertical column densities were retrieved using a two-step method from 28 July to 5 August of 2015 in Shanghai. The retrieved results were compared with the satellite products, and then their diurnal variation was observed. A consistency check was performed before the inversion to obtain a correction factor. Based on the sensitivity of geometric angles to oxygen dimer air mass factor (O4 AMF, AMF is the ratio of the slanted column density to the vertical column density), the parameterization scheme of geometric angles in the lookup table is optimized. The results show that the aerosol increased significantly in the afternoon. The diurnal variation of tropospheric NO2 and HCHO vertical column densities (VCDs) are bimodal and unimodal patterns respectively, and their values are higher than those of GOME-2 and OMI satellite products. A process of aerosol reduction and recovery are related to ground particulates and meteorological elements. The chemical sensitivity of local ozone production also has a clear diurnal variation.

Technical note: Evaluation of profile retrievals of aerosols and trace gases for MAX-DOAS measurements under different aerosol scenarios based on radiative transfer simulations

Abstract. Ground-based Multi-AXis Differential Optical Absorption Spectroscopy (MAX-DOAS) is a state-of-the-art remote sensing technique for deriving vertical profiles of trace gases and aerosols. However, MAX-DOAS profile inversions under aerosol pollution scenarios are challenging because of the complex radiative transfer and limited information content of the measurements. In this study, the performances of two inversion algorithms were evaluated for various aerosol pollution scenarios based on synthetic slant column densities (SCDs) derived from radiative transfer simulations. Compared to previous studies, in our study, much larger ranges of aerosol optical depth (AOD) and NO2 vertical column densities (VCDs) are covered. One inversion algorithm is based on optimal estimation; the other uses a parameterized approach. In this analysis, three types of profile shapes for aerosols and NO2 were considered: exponential, Boltzmann, and Gaussian. First, the systematic deviations of the retrieved aerosol profiles from the input profiles were investigated. For most cases, the AODs of the retrieved profiles were found to be systematically lower than the input values, and the deviations increased with increasing AOD. In particular for the optimal estimation algorithm and for high AOD, these findings are consistent with the results in previous studies. The assumed single scattering albedo (SSA) and asymmetry parameter (AP) have a systematic influence on the aerosol retrieval. However, for most cases the influence of the assumed SSA and AP on the retrieval results are rather small (compared to other uncertainties). For the optimal estimation algorithm, the agreement with the input values can be improved by optimizing the covariance matrix of the a priori uncertainties. Second, the aerosol effects on the NO2 profile retrieval were tested. Here, especially for the optimal estimation algorithm, a systematic dependence on the NO2 VCD was found, with a strong relative overestimation of the retrieved results for low NO2 VCDs and an underestimation for high NO2 VCDs. In contrast, the dependence on the aerosol profiles was found to be rather low. Interestingly, the results for both investigated wavelengths (360 and 477 nm) were found to be rather similar, indicating that the differences in the radiative transfer between both wavelengths have no strong effect. In general, both inversion schemes can retrieve the near-surface values of aerosol extinction and trace gas concentrations well.

Evaluation of UV–visible MAX-DOAS aerosol profiling products by comparison with ceilometer, sun photometer, and in situ observations in Vienna, Austria

Abstract. Since May 2017 and August 2018, two ground-based MAX-DOAS (multi-axis differential optical absorption spectroscopy) instruments have been continuously recording daytime spectral UV–visible measurements in the northwest (University of Natural Resources and Life Sciences (BOKU) site) and south (Arsenal site), respectively, of the Vienna city center (Austria). In this study, vertical aerosol extinction (AE) profiles, aerosol optical depth (AOD), and near-surface AE are retrieved from MAX-DOAS measurements recorded on cloud-free days applying the Bremen Optimal estimation REtrieval for Aerosols and trace gaseS (BOREAS) algorithm. Measurements of atmospheric profiles of pressure and temperature obtained from routinely performed sonde ascents are used to calculate box-air-mass factors and weighting functions for different seasons. The performance of BOREAS was evaluated against co-located ceilometer, sun photometer, and in situ instrument observations covering all four seasons. The results show that the vertical AE profiles retrieved from the BOKU UV–visible MAX-DOAS observations are in very good agreement with data from the co-located ceilometer, reaching correlation coefficients (R) of 0.936–0.996 (UV) and 0.918–0.999 (visible) during the fall, winter, and spring seasons. Moreover, AE extracted using the lowest part of MAX-DOAS vertical profiles (up to 100 m above ground) is highly consistent with near-surface ceilometer AE (R>0.865 and linear regression slopes of 0.815–1.21) during the fall, winter, and spring seasons. A strong correlation is also found for the BOREAS-based AODs when compared to the AERONET ones. Notably, the highest correlation coefficients (R=0.953 and R=0.939 for UV and visible, respectively) were identified for the fall season. While high correlation coefficients are generally found for the fall, winter, and spring seasons, the results are less reliable for measurements taken during summer. For the first time, the spatial variability of AOD and near-surface AE over the urban environment of Vienna is assessed by analyzing the retrieved and evaluated BOREAS aerosol profiling products in terms of different azimuth angles of the two MAX-DOAS instruments and for different seasons. We found that the relative differences of averaged AOD between different azimuth angles are 7–13 %, depending on the season. Larger relative differences of up to 32 % are found for near-surface AE in the different azimuthal directions. This study revealed the strong capability of BOREAS to retrieve AE profiles, AOD, and near-surface AE over urban environments and demonstrated its use for identifying the spatial variability of aerosols in addition to the temporal variation.

Evaluation of the LOTOS-EUROS NO<sub>2</sub> simulations using ground-based measurements and S5P/TROPOMI observations over Greece

Abstract. The evaluation of chemical transport models, CTMs, is essential for the assessment of their performance regarding the physical and chemical parameterizations used. While regional CTMs have been widely used and evaluated over Europe, their validation over Greece is limited. In this study, we investigate the performance of the Long Term Ozone Simulation European Operational Smog (LOTOS-EUROS) v2.2.001 regional chemical transport model in simulating nitrogen dioxide, NO2, over Greece from June to December 2018. In situ NO2 measurements obtained from 14 stations of the National Air Pollution Monitoring Network are compared with surface simulations over the two major cities of Greece, Athens and Thessaloniki. Overall the LOTOS-EUROS NO2 surface simulations compare very well to the in situ measurements showing a mild underestimation of the measurements with a mean relative bias of ∼-10 %, a high spatial correlation coefficient of 0.86 and an average temporal correlation of 0.52. The CTM underestimates the NO2 surface concentrations during daytime by ∼-50 ± 15 %, while it slightly overestimates during night-time ∼ 10 ± 35 %. Furthermore, the LOTOS-EUROS tropospheric NO2 columns are evaluated against ground-based multi-axis differential optical absorption spectroscopy (MAX-DOAS) NO2 measurements in Athens and Thessaloniki. We report that the CTM tropospheric NO2 column simulations over both urban and rural locations represent the diurnal patterns and hourly levels for both summer and winter seasons satisfactorily. The relative biases range between ∼ −2 % and −35 %, depending on season and relative NO2 load observed. Finally, the CTM was assessed also against space-borne Sentinel-5 Precursor (S5P) carrying the Tropospheric Monitoring Instrument (TROPOMI) tropospheric NO2 observations. We conclude that LOTOS-EUROS simulates extremely well the tropospheric NO2 patterns over the region with very high spatial correlation of 0.82 on average, ranging between 0.66 and 0.95, with negative biases in the summer and positive in the winter. Updated emissions for the simulations and model improvements when extreme values of boundary layer height are encountered are further suggested.

Measuring the Vertical Profiles of Aerosol Extinction in the Lower Troposphere by MAX-DOAS at a Rural Site in the North China Plain

Ground-based multi-axis differential optical absorption spectroscopy (MAX-DOAS) measurements were performed during the summer (13 June–20 August) of 2014 at a rural site in North China Plain. The vertical profiles of aerosol extinction (AE) in the lower troposphere were retrieved to analyze the temporal variations of AE profiles, near-surface AE, and aerosol optical depth (AOD). The average AOD and near-surface AE over the period of study were 0.51 ± 0.26 and 0.33 ± 0.18 km−1 during the effective observation period, respectively. High AE events and elevated AE layers were identified based on the time series of hourly AE profiles, near-surface AEs and AODs. It is found that in addition to the planetary boundary layer height (PBLH) and relative humidity (RH), the variations in the wind field have large impacts on the near-surface AE, AOD, and AE profile. Among 16 wind sectors, higher AOD or AE occur mostly in the directions of the cities upstream. The diurnal variations of the AE profiles, AODs and near-surface AEs are significant and influenced mainly by the source emissions, PBLH, and RH. The AE profile shape from MAX-DOAS measurement is generally in agreement with that from light detection and ranging (lidar) observations, although the AE absolute levels are different. Overall, ground-based MAX-DOAS can serve as a supplement to measure the AE vertical profiles in the lower troposphere.

MAX-DOAS measurements of NO<sub>2</sub>, SO<sub>2</sub>, HCHO, and BrO at the Mt. Waliguan WMO GAW global baseline station in the Tibetan Plateau

Abstract. Mt. Waliguan Observatory (WLG) is a World Meteorological Organization (WMO) Global Atmosphere Watch (GAW) global baseline station in China. WLG is located at the northeastern part of the Tibetan Plateau (36∘17′ N, 100∘54′ E, 3816 m a.s.l.) and is representative of the pristine atmosphere over the Eurasian continent. We made long-term ground-based multi-axis differential optical absorption spectroscopy (MAX-DOAS) measurements at WLG during the period 2012–2015. In this study, we retrieve the differential slant column densities (dSCDs) and estimate the tropospheric background mixing ratios of different trace gases, including NO2, SO2, HCHO, and BrO, using the measured spectra at WLG. Averaging of 10 original spectra is found to be an “optimum option” for reducing both the statistical error of the spectral retrieval and systematic errors in the analysis. The dSCDs of NO2, SO2, HCHO, and BrO under clear-sky and low-aerosol-load conditions are extracted from measured spectra at different elevation angles at WLG. By performing radiative transfer simulations with the model TRACY-2, we establish approximate relationships between the trace gas dSCDs at 1∘ elevation angle and the corresponding average tropospheric background volume mixing ratios. Mixing ratios of these trace gases in the lower troposphere over WLG are estimated to be in a range of about 7 ppt (January) to 100 ppt (May) for NO2, below 0.5 ppb for SO2, between 0.4 and 0.9 ppb for HCHO, and lower than 0.3 ppt for BrO. The chemical box model simulations constrained by the NO2 concentration from our MAX-DOAS measurements show that there is a little net ozone loss (−0.8 ppb d−1) for the free-tropospheric conditions and a little net ozone production (0.3 ppb d−1) for the boundary layer conditions over WLG during summertime. Our study provides valuable information and data sets for further investigating tropospheric chemistry in the background atmosphere and its links to anthropogenic activities.

Evaluation of the accuracy of the Sentinel-5 Precursor operational SO<sub>2</sub> products over China

The Sentinel-5 Precursor (S-5P) was launched into low earth orbit with a single payload TROPOspheric Monitoring Instrument (TROPOMI) on 13 October, 2017. TROPOMI is able to provide atmospheric composition observations including sulfur dioxide (SO2) daily and globally. It has a higher spatial resolution, specifically with a ground resolution of 7 km ×3.5 km in the nadir, than previous satellite instruments such as Ozone Monitoring Instrument (OMI, 13 km ×24 km) and Ozone Mapping and Profiler Suite (OMPS, 50 km ×50 km). The three types of S-5P operational SO2 products (offline (OFFL), Reprocessing (RPRO) and Near Real Time (NRTI)) are on basis of the differential optical absorption spectroscopy (DOAS) algorithm, and available from the S-5P Pre-Operations Data Hub. To evaluate these data, the results of OFFL are compared to the measurements obtained by ground-based Multi-Axis DOAS (MAX-DOAS) and China National Environmental Monitoring Center (CNEMC). We find that the S-5P operational SO2 products significantly overestimate SO2 concentrations over Northern China. Compared with four ground-based MAX-DOAS measurements in terms of the weekly average SO2 vertical column densities (VCDs), the S-5P operational SO2 products exhibit an overestimation of 61%−140%, with the correlation coefficient less than 0.5. The a priori SO2 profiles in S-5P operational products are from daily Tracer Model (TM5) simulations. SO2 surface concentrations are converted by the S-5P operational SO2 products and a priori SO2 profiles used in the retrievals. The correlation coefficient between the SO2 surface concentrations measured by CNEMC over Northern China and those from the S-5P operational products is higher than 0.5, and the S-5P operational products at these CNEMC sites show an overestimation of about 54.6% on average. In this study, the SO2 products (TROPOMI USTC SO2 products) are retrieved by the University of Science and Technology of China (USTC) with the optimal estimation algorithm (OE) from TROPOMI measurements, with the a priori SO2 profiles from monthly average GEOS-Chem simulations. The mean biases between the TROPOMI USTC SO2 products and the ground-based MAX-DOAS measurements are reduced significantly (−4.8%−22%), together with an improvement in the correlation coefficients (0.72−0.89). TROPOMI USTC SO2 surface concentrations are transformed by the TROPOMI USTC SO2 products and a priori SO2 profiles in the retrievals. Based on the evaluation statistics of the S-5P operational SO2 products, a smaller mean bias of −25.8% is found between the TROPOMI USTC SO2 surface concentrations and CNEMC measurements over Northern China. Compared to the TROPOMI USTC SO2 products in the heavily polluted area (33°−45°N, 110°−122°E), the S-5P operational SO2 products have an overestimation of around 41.3%, with a correlation coefficient of 0.73. In addition, S-5P operational SO2 products show a larger area of heavy pollution than TROPOMI USTC SO2 products. Additionally, the sensitivity analysis indicates many influential factors of the SO2 retrievals using OE algorithm, such as radiative calibration, fitting window and a priori SO2 profiles. In the fitting window of 310.5−326.0 nm, the SO2 columns retrieved by the a priori profiles from monthly GEOS-Chem simulations show better agreement with the MAX-DOAS measurements than those from daily TM5 simulations. A possible reason is that the emission inventory used in GEOS-Chem is based on a Chinese power sector database for 31 provinces supported by CMEP (Chinese Ministry of Environmental Protection), resulting in a better performance of GEOS-Chem than that of TM5 over China in simulations. And the overestimation of the S-5P operational SO2 products over Northern China may be attributed to the fitting window used.

First observation of tropospheric nitrogen dioxide from the Environmental Trace Gases Monitoring Instrument onboard the GaoFen-5 satellite

The Environmental Trace Gases Monitoring Instrument (EMI) is the first Chinese satellite-borne UV–Vis spectrometer aiming to measure the distribution of atmospheric trace gases on a global scale. The EMI instrument onboard the GaoFen-5 satellite was launched on 9 May 2018. In this paper, we present the tropospheric nitrogen dioxide (NO2) vertical column density (VCD) retrieval algorithm dedicated to EMI measurement. We report the first successful retrieval of tropospheric NO2 VCD from the EMI instrument. Our retrieval improved the original EMI NO2 prototype algorithm by modifying the settings of the spectral fit and air mass factor calculations to account for the on-orbit instrumental performance changes. The retrieved EMI NO2 VCDs generally show good spatiotemporal agreement with the satellite-borne Ozone Monitoring Instrument and TROPOspheric Monitoring Instrument (correlation coefficient R of ~0.9, bias < 50%). A comparison with ground-based MAX-DOAS (Multi-Axis Differential Optical Absorption Spectroscopy) observations also shows good correlation with an R of 0.82. The results indicate that the EMI NO2 retrieval algorithm derives reliable and precise results, and this algorithm can feasibly produce stable operational products that can contribute to global air pollution monitoring.

Vertical distributions of tropospheric formaldehyde, nitrogen dioxide, ozone and aerosol in southern China by ground-based MAX-DOAS and LIDAR measurements during PRIDE-GBA 2018 campaign

As the development of megacities, combined air pollution has been of increasing concern in China, which is composed by primary pollution, such as Nitrogen dioxide (NO2), and the followed secondary pollution under certain meteorology circumstances and high concentration of precursors, such as tropospheric ozone, formaldehyde (HCHO) and fine particles. During PRIDE-GBA 2018 Campaign (Particles, Radicals, Intermediates from oxiDation of primary Emissions in Great Bay Area), we performed the high resolution vertical observations of pollution gases and aerosol, which are significant but scarce indexes in studying the mechanisms of tropospheric pollution, using remote sensing techniques. NO2 and HCHO column densities and vertical profiles are reconstructed from data of multi-axis differential optical absorption spectroscopy (MAX-DOAS). Tropospheric ozone profile and aerosol extinction are retrieved by the differential absorption light detection and ranging (LIDAR) system. In order to verifying the accuracy, we evaluated the consistency and reliability of MAX-DOAS and LIDAR measurements. The results showed reasonable agreement with in-situ and off-line observations at Canton Tower. A typical combined pollution process from Sep 29 to Oct 10 was analyzed in detail. More than 200 μg/m3 tropospheric ozone in this case was considered from the anthropogenic sources, including industry, power plant, residential and transportation. The high emission from local industry and polluted air transport from northeast brought the main precursors of this pollution process. The photochemical formation of tropospheric ozone was turned into a VOC-limited regime on polluted days.

A new method to determine the aerosol optical properties from multiple-wavelength O&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt; absorptions by MAX-DOAS observation

Abstract. Ground-based multi-axis differential optical absorption spectroscopy (MAX-DOAS) observation was carried out from November 2016 to February 2017 in Beijing, China, to measure the O4 absorptions in UV and visible bands and further to illustrate its relationship with aerosol optical properties (AOPs) under different weather types. According to relative humidity, visibility, and PM2.5, we classified the observation periods into clear, light-haze, haze, heavy-haze, fog, and rainy weather conditions. There are obvious differences for measured AOPs under different weather conditions, especially scattering coefficient (σsca) and absorption coefficient (σsca). It was also found that both the O4 differential slant column densities (DSCDs) at the UV and visible bands varied in the order of clear days &gt; light-haze days &gt; haze days &gt; heavy-haze days &gt; fog days. The correlation coefficients (R2) between O4 DSCDs at 360.8 and 477.1 nm mainly varied in the order of clear days &gt; light-haze days &gt; haze days &gt; heavy-haze days. Based on the statistics of O4 DSCDs at an elevation angle 1∘ with the corresponding linear regression between UV and visible bands of segmental periods, the relationships between O4 DSCDs and AOPs were established. It should mainly be clear or light-haze days when the correlation slope is greater than 1.0, with a correlation coefficient (R2) greater than 0.9, and O4 DSCDs mainly greater than 2.5×1043 molec. cm−2. Meanwhile, σsca and σabs are less than 45 and 12 Mm−1, respectively. For haze or heavy-haze days, the correlation slope is less than 0.6, with an R2 less than 0.8, and O4 DSCDs mainly less than 1.3×1043 molec. cm−2, under which σsca and σabs are mainly located at 200–900 and 20–60 Mm−1. Additionally, the determination method was well validated based on another MAX-DOAS measurement at Gucheng from 19 to 27 November 2016. For more precise and accurate inversion of AOPs, more detailed look-up tables for O4 multiple-wavelength absorptions need to be developed. Since the ground surface AOPs were determined using MAX-DOAS observation at a 1∘ elevation in this study, we hope to highlight the potential of retrieved vertical spatially resolved AOPs being expected when multiple elevation angles of MAX-DOAS observation are used together.

Observations and source investigations of the boundary layer bromine monoxide (BrO) in the Ny-Ålesund Arctic

Abstract. During polar spring, the presence of reactive bromine in the polar boundary layer is considered to be the main cause of ozone depletion and mercury deposition. However, many uncertainties still remain regarding understanding the mechanisms of the chemical process and source of the bromine. As Arctic sea ice has recently been dramatically reduced, it is critical to investigate the mechanisms using more accurate measurements with higher temporal and spatial resolution. In this study, a typical process of enhanced bromine and depleted ozone in the Ny-Ålesund boundary layer in late April 2015 was observed by applying ground-based multi-axis differential optical absorption spectroscopy (MAX-DOAS) technique. The results showed that there were bromine monoxide (BrO) slant columns as high as 5.6 × 1014 molec cm−2 above the Kings Bay area on 26 April. Meanwhile, the boundary layer ozone and gaseous elemental mercury (GEM) were synchronously reduced by 85 and 90 %, respectively. Based on the meteorology, sea ice distribution and air mass history, the sea ice in the Kings Bay area, which emerged for only a very short period of time when the enhanced BrO was observed, was considered to be the major source of this bromine enhancement event. The oxidized GEM may be directly deposited onto snow/ice and thereby influence the polar ecosystem.

Evaluation of MAX-DOAS aerosol retrievals by coincident observations using CRDS, lidar, and sky radiometer inTsukuba, Japan

Abstract. Coincident aerosol observations of multi-axis differential optical absorption spectroscopy (MAX-DOAS), cavity ring-down spectroscopy (CRDS), lidar, and sky radiometer were conducted in Tsukuba, Japan, on 5–18 October 2010. MAX-DOAS aerosol retrieval (for aerosol extinction coefficient and aerosol optical depth at 476 nm) was evaluated from the viewpoint of the need for a correction factor for oxygen collision complexes (O4 or O2–O2) absorption. The present study strongly supports this need, as systematic residuals at relatively high elevation angles (20 and 30°) were evident in MAX-DOAS profile retrievals conducted without the correction. However, adopting a single number for the correction factor (fO4 = 1.25) for all of the elevation angles led to systematic overestimation of near-surface aerosol extinction coefficients, as reported in the literature. To achieve agreement with all three observations, we limited the set of elevation angles to ≤10° and adopted an elevation-angle-dependent correction factor for practical profile retrievals with scattered light observations by a ground-based MAX-DOAS. With these modifications, we expect to minimize the possible effects of temperature-dependent O4 absorption cross section and uncertainty in DOAS fit on an aerosol profile retrieval, although more efforts are encouraged to quantitatively identify a physical explanation for the need of a correction factor.

Spatiotemporal inhomogeneity in NO2 over Fukuoka observed by ground-based MAX-DOAS

Continuous NO2 profile observations have been made using ground-based Multi-Axis Differential Optical Absorption Spectroscopy (MAX-DOAS) at Fukuoka (33.55°N, 130.36°E), an urban area in Japan. Throughout the year, NO2 variations measured by MAX-DOAS (0–100 m) are in good agreement with in situ surface NO2 measurements on several-day, week-to-week, and seasonal timescales. We investigated the spatiotemporal inhomogeneity in NO2 over Fukuoka by observing at two azimuth angles: the Tenjin (towards the city center) and Itoshima (away from the city center) directions. In terms of diurnal variations, NO2 in both directions show clear morning maxima, on account of local emissions in the morning and the development of a boundary layer. The concentrations in the early morning are nearly the same in both directions, but they are higher in the Tenjin direction during most of the daytime on average. Variability in both directions, as well as spatial inhomogeneity, is large during most of the daytime except for in the morning. The diurnal maximum for 0–1 km between 10 and 13 LT is sometimes observed in the Tenjin direction; in some cases, 1 h after this maximum, a maximum is also observed in the Itoshima direction. The NO2 maxima for the upper level (1–2 km) in both directions are also delayed from the maximum in the Tenjin direction for 0–1 km. Analysis of the surface wind field indicates that the NO2 inhomogeneity is strongly related to vertical/horizontal transport of high concentrations of NO2 from the city center, and to horizontal transport of low concentrations from the ocean via a land–sea breeze. Three-dimensional continuous observations by MAX-DOAS are potentially a powerful tool for increasing our understanding of pollutant transport and mixing in urban areas.

Intercomparison of slant column measurements of NO2 by ground-based MAX-DOAS

In September 2011, we used 3 ground-based multi-axis differential optical absorption spectroscopy (MAX-DOAS) instruments of different designs and operation protocols to measure tropospheric NO2 for about 20 days, at the Station of Atmospheric Comprehensive Observatory, Institute of Atmospheric Physics, Chinese Academy of Sciences (Xianghe 117.0N, 39.77E). All instruments are oriented to an azimuth angle of 270 (north), in a common wavelength range and with a set of cross sections for the inversion of NO2 slant column in visible and UV wavelength range respectively. Intercomparison of NO2 slant columns among three MAX-DOAS is introduced. The results obtained from the different instruments are in good accordance with each other, and the correlation coefficients are all higher than 0.95, but systematical errors exist. Daily average errors of three MAX-DOAS instruments are almost below 6%, showing that the instruments work steadily and the data are cogent. The UV results are smaller than those in the visible range, especially on the overcast days, related to the wavelength dependence of Rayleigh and Mie scattering. After the correction of systematical errors, there is better consistency among different results, which indicates that the three MAX-DOAS instruments have a capability to validate the atmospheric component products of satellite.