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Abstract. The satellite instruments Optical Transient Detector (OTD) and Lightning Imaging Sensor (LIS) provide unique empirical data about the frequency of lightning flashes around the globe (OTD), and the tropics (LIS), which have been used before to compile a well-received global climatology of flash rate densities. Here we present a statistical analysis of various additional lightning properties derived from OTD / LIS, i.e., the number of so-called "events" and "groups" per flash, as well as the mean flash duration, footprint and radiance. These normalized quantities, which can be associated with the flash "strength", show consistent spatial patterns; most strikingly, oceanic flashes show higher values than continental flashes for all properties. Over land, regions with high (eastern US) and low (India) flash strength can be clearly identified. We discuss possible causes for and implications of the observed regional differences. Although a direct quantitative interpretation of the investigated flash properties is difficult, the observed spatial patterns provide valuable information for the interpretation and application of climatological flash rates. Due to the systematic regional variations of physical flash characteristics, viewing conditions, and/or measurement sensitivities, parametrizations of lightning NOx based on total flash rate densities alone are probably affected by regional biases.

Nitrogen oxides, released from fossil fuel use and other combustion processes, affect air quality and climate. From the mid-1990s onward, nitrogen dioxide (NO2) has been monitored from space, and since 2004 with relatively high spatial resolution by the Ozone Monitoring Instrument. Strong upward NO2 trends have been observed over South and East Asia and the Middle East, in particular over major cities. We show, however, that a combination of air quality control and political factors, including economical crisis and armed conflict, has drastically altered the emission landscape of nitrogen oxides in the Middle East. Large changes, including trend reversals, have occurred since about 2010 that could not have been predicted and therefore are at odds with emission scenarios used in projections of air pollution and climate change in the early 21st century.

14 pags., 10 figs. ; Iodine plays a vital role in oxidation chemistry over Antarctica, with past observations showing highly elevated levels of iodine oxide (IO) leading to severe depletion of boundary layer ozone in West Antarctica. Here, we present MAX-DOAS-based (multi-axis differential absorption spectroscopy) observations of IO over three summers (2015-2017) at the Indian Antarctic bases of Bharati and Maitri. IO was observed during all the campaigns with mixing ratios below 2ĝ€¯pptv (parts per trillion by volume) for the three summers, which are lower than the peak levels observed in West Antarctica. This suggests that sources in West Antarctica are different or stronger than sources of iodine compounds in East Antarctica, the nature of which is still uncertain. Vertical profiles estimated using a profile retrieval algorithm showed decreasing gradients with a peak in the lower boundary layer. The ground-based instrument retrieved vertical column densities (VCDs) were approximately a factor of 3 to 5 higher than the VCDs reported using satellite-based instruments, which is most likely related to the sensitivities of the measurement techniques. Air mass back-trajectory analysis failed to highlight a source region, with most of the air masses coming from coastal or continental regions. This study highlights the variation in iodine chemistry in different regions in Antarctica and the importance of a long-term dataset to validate models estimating the impacts of iodine chemistry. ; The ISEA campaigns are organized by the National Centre for Polar and Ocean Research (NCPOR), Ministry of Earth Sciences (MOES), Government of India.IITM and NCPOR are funded by MOES, Government of India.

Recently it was discovered that over the Middle East during summer ozone mixing ratios can reach a pronounced maximum in the middle troposphere. Here we extend the analysis to the surface and show that especially in the Persian Gulf region conditions are highly favorable for ozone air pollution. We apply the EMAC atmospheric chemistry-climate model to investigate long-distance transport and the regional formation of ozone. Further, we make use of available in situ and satellite measurements and compare these with model output. The results indicate that the region is a hot spot of photochemical smog where European Union air quality standards are violated throughout the year. Long-distance transports of air pollution from Europe and the Middle East, natural emissions and stratospheric ozone conspire to bring about relatively high background ozone mixing ratios. This provides a hotbed to strong and growing indigenous air pollution in the dry local climate, and these conditions are likely to get worse in the future.

International audience ; Recently it was discovered that over the Middle East during summer ozone mixing ratios can reach a pronounced maximum in the middle troposphere. Here we extend the analysis to the surface and show that especially in the Persian Gulf region conditions are highly favorable for ozone air pollution. We apply the EMAC atmospheric chemistry-climate model to investigate long-distance transport and the regional formation of ozone. Further, we make use of available in situ and satellite measurements and compare these with model output. The results indicate that the region is a hot spot of photochemical smog where European Union air quality standards are violated throughout the year. Long-distance transports of air pollution from Europe and the Middle East, natural emissions and stratospheric ozone conspire to bring about relatively high background ozone mixing ratios. This provides a hotbed to strong and growing indigenous air pollution in the dry local climate, and these conditions are likely to get worse in the future.

International audience ; Recently it was discovered that over the Middle East during summer ozone mixing ratios can reach a pronounced maximum in the middle troposphere. Here we extend the analysis to the surface and show that especially in the Persian Gulf region conditions are highly favorable for ozone air pollution. We apply the EMAC atmospheric chemistry-climate model to investigate long-distance transport and the regional formation of ozone. Further, we make use of available in situ and satellite measurements and compare these with model output. The results indicate that the region is a hot spot of photochemical smog where European Union air quality standards are violated throughout the year. Long-distance transports of air pollution from Europe and the Middle East, natural emissions and stratospheric ozone conspire to bring about relatively high background ozone mixing ratios. This provides a hotbed to strong and growing indigenous air pollution in the dry local climate, and these conditions are likely to get worse in the future.

International audience ; Recently it was discovered that over the Middle East during summer ozone mixing ratios can reach a pronounced maximum in the middle troposphere. Here we extend the analysis to the surface and show that especially in the Persian Gulf region conditions are highly favorable for ozone air pollution. We apply the EMAC atmospheric chemistry-climate model to investigate long-distance transport and the regional formation of ozone. Further, we make use of available in situ and satellite measurements and compare these with model output. The results indicate that the region is a hot spot of photochemical smog where European Union air quality standards are violated throughout the year. Long-distance transports of air pollution from Europe and the Middle East, natural emissions and stratospheric ozone conspire to bring about relatively high background ozone mixing ratios. This provides a hotbed to strong and growing indigenous air pollution in the dry local climate, and these conditions are likely to get worse in the future.

International audience ; Recently it was discovered that over the Middle East during summer ozone mixing ratios can reach a pronounced maximum in the middle troposphere. Here we extend the analysis to the surface and show that especially in the Persian Gulf region conditions are highly favorable for ozone air pollution. We apply the EMAC atmospheric chemistry-climate model to investigate long-distance transport and the regional formation of ozone. Further, we make use of available in situ and satellite measurements and compare these with model output. The results indicate that the region is a hot spot of photochemical smog where European Union air quality standards are violated throughout the year. Long-distance transports of air pollution from Europe and the Middle East, natural emissions and stratospheric ozone conspire to bring about relatively high background ozone mixing ratios. This provides a hotbed to strong and growing indigenous air pollution in the dry local climate, and these conditions are likely to get worse in the future.

Recently it was discovered that over the Middle East during summer ozone mixing ratios can reach a pronounced maximum in the middle troposphere. Here we extend the analysis to the surface and show that especially in the Persian Gulf region conditions are highly favorable for ozone air pollution. We apply the EMAC atmospheric chemistry-climate model to investigate long-distance transport and the regional formation of ozone. Further, we make use of available in situ and satellite measurements and compare these with model output. The results indicate that the region is a hot spot of photochemical smog where European Union air quality standards are violated throughout the year. Long-distance transports of air pollution from Europe and the Middle East, natural emissions and stratospheric ozone conspire to bring about relatively high background ozone mixing ratios. This provides a hotbed to strong and growing indigenous air pollution in the dry local climate, and these conditions are likely to get worse in the future.

30 pags., 13 figs., 4 tabs. ; We present the inter-comparison of delta slant column densities (SCDs) and vertical profiles of nitrous acid (HONO) derived from measurements of different multiaxis differential optical absorption spectroscopy (MAXDOAS) instruments and using different inversion algorithms during the Second Cabauw Inter-comparison campaign for Nitrogen Dioxide measuring Instruments (CINDI- 2) in September 2016 at Cabauw, the Netherlands (51.97° N, 4.93° E). The HONO vertical profiles, vertical column densities (VCDs), and near-surface volume mixing ratios are compared between different MAX-DOAS instruments and profile inversion algorithms for the first time. Systematic and random discrepancies of the HONO results are derived from the comparisons of all data sets against their median values. Systematic discrepancies of HONO delta SCDs are observed in the range of ±0:3×1015 molec. cm2, which is half of the typical random discrepancy of 0:6× 1015 molec. cm2. For a typical high HONO delta SCD of 2×1015 molec. cm2, the relative systematic and random discrepancies are about 15% and 30 %, respectively. The inter-comparison of HONO profiles shows that both systematic and random discrepancies of HONO VCDs and nearsurface volume mixing ratios (VMRs) are mostly in the range of ∼ ±0:5×1014 molec. cm2 and ∼ ±0:1 ppb (typically ∼ 20 %). Further we find that the discrepancies of the retrieved HONO profiles are dominated by discrepancies of the HONO delta SCDs. The profile retrievals only contribute to the discrepancies of the HONO profiles by ∼ 5 %. However, some data sets with substantially larger discrepancies than the typical values indicate that inappropriate implementations of profile inversion algorithms and configurations of radiative transfer models in the profile retrievals can also be an important uncertainty source. In addition, estimations of measurement uncertainties of HONO dSCDs, which can significantly impact profile retrievals using the optimal estimation method, need to consider not only DOAS fit errors, but also atmospheric variability, especially for an instrument with a DOAS fit error lower than ∼ 3×1014 molec. cm2. The MAX-DOAS results during the CINDI-2 campaign indicate that the peak HONO levels (e.g. near-surface VMRs of ∼ 0:4 ppb) often appeared in the early morning and below 0.2 km. The near-surface VMRs retrieved from the MAXDOAS observations are compared with those measured using a co-located long-path DOAS instrument. The systematic differences are smaller than 0.15 and 0.07 ppb during early morning and around noon, respectively. Since true HONO values at high altitudes are not known in the absence of real measurements, in order to evaluate the abilities of profile inversion algorithms to respond to different HONO profile shapes, we performed sensitivity studies using synthetic HONO delta SCDs simulated by a radiative transfer model with assumed HONO profiles. The tests indicate that the profile inversion algorithms based on the optimal estimation method with proper configurations can reproduce the different HONO profile shapes well. Therefore we conclude that the features of HONO accumulated near the surface derived from MAX-DOAS measurements. ; Funding for this study was provided by ESA through the CINDI-2 (ESA contract no. 4000118533/16/I-Sbo) and FRM4DOAS (ESA contract no. 4000118181/16/I-EF) projects, by the NSFC (grant no. 41805027), the Russian Foundation for Basic Research (grant no. 18-35-00682), the Russian Academy of Sciences (grant nos. 0150-2018-0052 and 0129-2019- 0002), NASA's Atmospheric Composition Program (grant no. NASA-16-NUP2016-0001), the US National Science Foundation (AGS-1620530 award), and the European Union's Horizon 2020 research and innovation programme through the ACTRIS-2 transnational access programme (grant no. 654109). The AIOFM group is grateful for the support by the NSFC (grant no. 41530644). The article processing charges for this open-access publication were covered by the Max Planck Society