8 results on '"Künstler, Christopher"'
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2. O3 formation sensitivity to precursors and lightning in the tropical troposphere based on airborne observations
- Author
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Nussbaumer, Clara Maria, primary, Kohl, Matthias, additional, Pozzer, Andrea, additional, Tadic, Ivan, additional, Rohloff, Roland, additional, Marno, Daniel, additional, Harder, Hartwig, additional, Ziereis, Helmut Alois, additional, Zahn, Andreas, additional, Obersteiner, Florian, additional, Hofzumahaus, Andreas, additional, Fuchs, Hendrik, additional, Künstler, Christopher, additional, Brune, William H., additional, Ryerson, Thomas B., additional, Peischl, Jeff, additional, Thompson, Chelsea, additional, Bourgeois, Ilann, additional, Lelieveld, Jos, additional, and Fischer, Horst, additional
- Published
- 2024
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3. Ozone Formation Sensitivity to Precursors and Lightning in the Tropical Troposphere Based on Airborne Observations.
- Author
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Nussbaumer, Clara M., Kohl, Matthias, Pozzer, Andrea, Tadic, Ivan, Rohloff, Roland, Marno, Daniel, Harder, Hartwig, Ziereis, Helmut, Zahn, Andreas, Obersteiner, Florian, Hofzumahaus, Andreas, Fuchs, Hendrik, Künstler, Christopher, Brune, William H., Ryerson, Tom B., Peischl, Jeff, Thompson, Chelsea R., Bourgeois, Ilann, Lelieveld, Jos, and Fischer, Horst
- Subjects
TRACE gases ,PEROXY radicals ,ATMOSPHERIC models ,TROPOSPHERE ,AIR pollutants ,TROPOSPHERIC ozone ,NITROGEN oxides ,TROPOSPHERIC chemistry - Abstract
Tropospheric ozone (O3) is an important greenhouse gas that is also hazardous to human health. The formation of O3 is sensitive to the levels of its precursors NOx (≡NO + NO2) and peroxy radicals, for example, generated by the oxidation of volatile organic compounds (VOCs). A better understanding of this sensitivity will show how changes in the levels of these trace gases could affect O3 levels today and in the future, and thus air quality and climate. In this study, we investigate O3 sensitivity in the tropical troposphere based on in situ observations of NO, HO2 and O3 from four research aircraft campaigns between 2015 and 2023. These are OMO (Oxidation Mechanism Observations), ATom (Atmospheric Tomography Mission), CAFE Africa (Chemistry of the Atmosphere Field Experiment in Africa) and CAFE Brazil, in combination with simulations using the EMAC atmospheric chemistry—climate model. We use the metric α(CH3O2) together with NO to investigate the O3 formation sensitivity. We show that O3 formation is generally NOx‐sensitive in the lower and middle tropical troposphere and is in a transition regime in the upper troposphere. By distinguishing observations impacted by lightning or not we show that NO from lightning is the most important driver of O3 sensitivity in the tropics. NOx‐sensitive chemistry predominates in regions without lightning impact, with α(CH3O2) ranging between 0.56 and 0.82 and observed average O3 levels between 35 and 55 ppbv. Areas affected by lightning exhibit strongly VOC‐sensitive O3 chemistry with α(CH3O2) of about 1 and average O3 levels between 55 and 80 ppbv. Plain Language Summary: Ozone (O3) in the troposphere is both an air pollutant and a greenhouse gas. It is formed from nitrogen oxides (NOx) and volatile organic compounds (VOCs). The formation can be sensitive to either of these precursors depending on their abundance. Considering the high relevance of O3 in regard to human health and global warming, it is important to understand this sensitivity of O3 formation, which allows to predict future changes in O3. Here, we investigate O3 formation sensitivity toward NOx and VOCs in the tropical troposphere based on aircraft measurements during four research campaigns between 2015 and 2023, and a global model. We include observations of NO, HO2 (hydroperoxyl radicals) and O3 over South America, the Middle East and the Pacific, Atlantic and Indian Ocean. We find that O3 formation is sensitive to NOx in the lower tropical troposphere. In the upper tropical troposphere, lightning events control O3 chemistry and promote strong VOC‐sensitive O3 formation. Key Points: α(CH3O2) correlated with NO is a powerful metric for indicating O3 sensitivity and is valid throughout the troposphereO3 chemistry in the remote tropical lower troposphere is found to be NOx‐sensitiveNO emissions from lightning drive O3 sensitivity in the tropical upper troposphere and induce highly VOC‐sensitive chemistry [ABSTRACT FROM AUTHOR]
- Published
- 2024
- Full Text
- View/download PDF
4. Poisson–Cournot games
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De Sinopoli, Francesco, primary, Künstler, Christopher, additional, Meroni, Claudia, additional, and Pimienta, Carlos, additional
- Published
- 2022
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5. Measurements of Atmospheric OH and HO2 Radicals by Laser-Induced Fluorescence on the HALO Aircraft during the OMO-ASIA 2015 Campaign
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Künstler, Christopher
- Subjects
ddc:540 ,ddc:000 ,ddc:530 ,ddc:500 - Abstract
The goal of this work was to investigate the chemistry of atmospheric OH and HO2 radicals in the upper troposphere during the Asian summer monsoon period 2015 within the Oxidation Mechanism Observation (OMO) campaign. Concentrations of OH and HO2 were measured by a laser-induced fluorescence instrument (AirLIF) on the German research aircraft HALO between the Mediterranean Sea and the Maldives in the Indian Ocean. The measured data are compared to theoretical model predictions in order to test the understanding of atmospheric oxidation processes. For this purpose the precedingly developed AirLIF instrument at Forschungszentrum Jülich was thoroughly characterized in the laboratory and different calibration concepts applied and compared. The radical measurements during OMO were then evaluated and a zero-dimensional chemical box-model calculation for the expected OH and HO2 radical concentrations was tested against the measurement results. For the radical measurements using the AirLIF instrument on HALO, the ambient air is first sampled and decelerated by a factor of 10 inside a shrouded inlet (designed and built at Forschungszentrum Jülich). The air is then expanded into a measurement cell at low pressure inside the aircraft, where OH is detected by laser excited fluorescence. The OH and HO2 channel of AirLIF needed to be characterized for the flight conditions during OMO. Different calibration concepts have been applied and combined to determine the OH and HO2 detection sensitivities as a function of flight altitude, ambient pressure and temperature. These include the well established ground-based calibrations between flights to track the absolute sensitivities. The relative dependence with altitude was measured in the laboratory using a newly designed photochemical radical source which allows calibration at reduced pressure to simulate ambient air pressure at flight conditions. For the OH-channel - as an additional option - an in-flight calibration unit inside the shrouded inlet was used. It is however limited to below 10 km, because the radical production by the artificial photolysis of ambient water vapour becomes too small. To simulate the in-flight conditions, other research groups have confided in using different nozzle sizes to change the mass-flow through the system instead of varying ambient pressure. As part of a consistency check, both methods have been compared in detail and it is confirmed that they essentially agree. However, discontinuities in the pressure dependence of the OH calibration curve are presumably related to a change in conditions of the gas expansion and are thereby unique to a specific nozzle. The correct detection of this jump in sensitivity is therefore limited to the newly developed radical source. During the laboratory characterization of the HO2 channel a fluid dynamical effect on the HO2 nozzle was discovered, which is due to the lacking shrouded inlet and led to an overestimated HO2 inlet pressure, originally assumed to be static ambient pressure. It was possible to correct this by calculating the true mass flow through the nozzle using the computational fluid dynamics (CFD) software ANSYS Fluent. The OMO campaign took place from 21 July until 27 August 2015 and was divided in three phases. Till 01 August 2015 HALO was stationed on the airport of Paphos (Cyprus) and mainly flew over Cyprus and the Mediterranean Sea. During the second phase HALO was stationed on Gan (Maldives) aiming for the flight targets Bahrain and Sri Lanka, west and east of India respectively. From 10 August till the end of the campaign, HALO was again stationed on Cyprus and covered the Arabian Peninsula, Egypt and Greece as primary flight targets. At the end of the campaign for two flights Mount Etna was visited. In total OMO Asia comprised 17 flights up to 15 km of which AirLIF measured 2/3 of the time. Other institutes involved in OMO were the Karlsruhe Institute of Technology (KIT), the German Aerospace Center (DLR), the Max-Planck Institute for Chemistry (MPIC Mainz) and the universities Bremen, Wuppertal, Heidelberg and Leipzig. The MPIC Mainz provided a second LIF instrument measuring OH and HO2 radicals contemporaneously for the first time. Both, AirLIF and HORUS OH and HO2 in-flight measurements are intercompared flight-wise showing a general good agreement of their calibrations. The vertical profile of OH and HO2 up to 15 km is discussed in particular with respect to important atmospheric controlling parameters such as CO and NO. The HO2/OH ratio is then analyzed by a simple analytic approach. It is found that the latter is well explained above 7 km, while below a gap of a factor up to 3 remains. The altitude profiles and oxidation processes are further studied by using a zero-dimensional chemical box-model which is constrained by parameters measured by other instruments during the OMO campaign. Good agreement of OH and HO2 is found between 7 km and 11.5 km, while below 7 km OH is overestimated by a factor of 2.5 and HO2 is predicted correctly within the combined model-measurement uncertainty. This result is consistent with the underestimation of the HO2/OH ratio by up to a factor of 3 which is in agreement by the analytical model. Above 11.5 km both, OH and HO2, are overestimated by a factor up to 2.5. In the HO2/OH ratio however, this overestimation cancels out which indicates that there is either a missing HOx termination reaction or an overestimated HOx primary source in the model. The discrepancies observed in the upper and lower troposphere are finally addressed by sensitivity studies. In the lower troposphere these are most likely due to missing VOC reactivity, which primarily acts as an OH sink. The addition of a small amount of OH reactivity (0.1 s-1) due to unmeasured VOCs during the OMO Asia campaign, closed the gap for OH, while HO2 stayed in agreement. Only below 2 km a discrepancy of the HO2/OH ratio by a factor up to 2.5 remained. In the upper troposphere there are indications, that formaldehyde from the EMAC MPIC model is overestimated, which results in a contemporaneous increase in OH and HO2. This work, in particular the correction necessary to the HO2 channel, hints to further technical improvements for prospective LIF-aircraft applications.
- Published
- 2020
6. LIF instrument for airborne measurements of OH, HO2 and RO2 radicals in the upper troposphere deployed on HALO during the OMO 2015 campaign
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Künstler, Christopher, Broch, Sebastian, Zöger, Martin, Wahner, Andreas, Bachner, Mathias, Bayer, Norbert, Dahlhoff, Knut, Fuchs, Hendrik, Holland, Frank, Hofzumahaus, Andreas, Jansen, Peter, and Wolters, Jörg
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ddc:550 - Published
- 2016
7. Investigation of potential interferences in the detection of atmospheric RO<sub><i>x</i></sub> radicals by laser-induced fluorescence under dark conditions
- Author
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Fuchs, Hendrik, primary, Tan, Zhaofeng, additional, Hofzumahaus, Andreas, additional, Broch, Sebastian, additional, Dorn, Hans-Peter, additional, Holland, Frank, additional, Künstler, Christopher, additional, Gomm, Sebastian, additional, Rohrer, Franz, additional, Schrade, Stephanie, additional, Tillmann, Ralf, additional, and Wahner, Andreas, additional
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- 2016
- Full Text
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8. Investigation of potential interferences in the detection of atmospheric ROx radicals by laser-induced fluorescence under dark conditions.
- Author
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Fuchs, Hendrik, Zhaofeng Tan, Hofzumahaus, Andreas, Broch, Sebastian, Dorn, Hans-Peter, Holland, Frank, Künstler, Christopher, Gomm, Sebastian, Rohrer, Franz, Schrade, Stephanie, Tillmann, Ralf, and Wahner, Andreas
- Subjects
HYDROXYL group ,CHEMICAL radical spectra ,ATMOSPHERIC hydroxyl radicals ,FLUORESCENCE spectroscopy ,LASER beams ,VOLUMETRIC analysis ,RADICALS (Chemistry) ,EQUIPMENT & supplies - Abstract
Direct detection of highly reactive, atmospheric hydroxyl radicals (OH) is widely accomplished by laserinduced fluorescence (LIF) instruments. The technique is also suitable for the indirect measurement of HO
2 and RO2 peroxy radicals by chemical conversion to OH. It requires sampling of ambient air into a low-pressure cell, where OH fluorescence is detected after excitation by 308 nm laser radiation. Although the residence time of air inside the fluorescence cell is typically only on the order of milliseconds, there is potential that additional OH is internally produced, which would artificially increase the measured OH concentration. Here, we present experimental studies investigating potential interferences in the detection of OH and peroxy radicals for the LIF instruments of Forschungszentrum Jülich for nighttime conditions. For laboratory experiments, the inlet of the instrument was over flowed by excess synthetic air containing one or more reactants. In order to distinguish between OH produced by reactions upstream of the inlet and artificial signals produced inside the instrument, a chemical titration for OH was applied. Additional experiments were performed in the simulation chamber SAPHIR where simultaneous measurements by an open-path differential optical absorption spectrometer (DOAS) served as reference for OH to quantify potential artifacts in the LIF instrument. Experiments included the investigation of potential interferences related to the nitrate radical (NO3 , N2 O5 ), related to the ozonolysis of alkenes (ethene, propene, 1-butene, 2,3-dimethyl-2-butene, α-pinene, limonene, isoprene), and the laser photolysis of acetone. Experiments studying the laser photolysis of acetone yield OH signals in the fluorescence cell, which are equivalent to 0:05 106 cm-3 OH for a mixing ratio of 5 ppbv acetone. Under most atmospheric conditions, this interference is negligible. No significant interferences were found for atmospheric concentrations of reactants during ozonolysis experiments. Only for propene, α-pinene, limonene, and isoprene at reactant concentrations, which are orders of magnitude higher than in the atmosphere, could artificial OH be detected. The value of the interference depends on the turnover rate of the ozonolysis reaction. For example, an apparent OH concentration of approximately 1 106 cm-3 is observed when 5.8 ppbv limonene reacts with 600 ppbv ozone. Experiments with the nitrate radical NO3 reveal a small interference signal in the OH, HO2 , and RO2 detection. Dependencies on experimental parameters point to artificial OH formation by surface reactions at the chamber walls or in molecular clusters in the gas expansion. The signal scales with the presence of NO3 giving equivalent radical concentrations of 1:1 105 cm-3 OH, 1 107 cm-3 HO2 , and 1:7 107 cm-3 RO2 per 10 pptv NO3 . [ABSTRACT FROM AUTHOR]- Published
- 2016
- Full Text
- View/download PDF
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