scholarly journals Diurnal variation in middle atmospheric ozone by ground based microwave radiometry at Ny-Ålesund over 1 year

2017 ◽  
Author(s):  
Franziska Schranz ◽  
Susana Fernandez ◽  
Niklaus Kämpfer ◽  
Mathias Palm
Keyword(s):  
Diurnal Cycle ◽  
Reaction Rates ◽  
Ozone Production ◽  
The Arctic ◽  
High Time Resolution ◽  
Atmospheric Ozone ◽  
Polar Day ◽  
One Year ◽  
Microwave Radiometers ◽  
Chemical Reaction Rates

Abstract. We present an analysis of the diurnal ozone cycle from one year of continuous ozone measurements from two ground based microwave radiometers in the Arctic. The instruments GROMOS-C and OZORAM have been located at the AWIPEV research base at Ny-Ålesund, Svalbard (79° N, 12° E) and gathered a comprehensive time series of middle atmospheric ozone profiles with a high time resolution. An intercomparison was performed with EOS MLS and ozone sonde measurements and simulations with SD-WACCM. The measured datasets were used to study the photochemically induced diurnal cycle of ozone in the stratosphere and mesosphere. Throughout the year the insolation in the Arctic changes drastically from polar night to polar day. Accordingly, the seasonal variations in the diurnal ozone cycle are large. In the stratosphere we found a diurnal cycle throughout the whole period of polar day with the largest amplitude in April. In the mesosphere a diurnal cycle was detected in spring and fall. SD-WACCM has proved to well capture the diurnal cycle and was therefore used to analyse the chemical reaction rates of ozone production and loss at equinox and summer solstice. Furthermore GROMOS-C proofed capable of measuring the tertiary ozone layer above Ny-Ålesund in winter.

scholarly journals Diurnal variation in middle-atmospheric ozone observed by ground-based microwave radiometry at Ny-Ålesund over 1 year

2018 ◽  
Vol 18 (6) ◽  
pp. 4113-4130 ◽  
Author(s):  
Franziska Schranz ◽  
Susana Fernandez ◽  
Niklaus Kämpfer ◽  
Mathias Palm
Keyword(s):  
Diurnal Cycle ◽  
Reaction Rates ◽  
Ozone Production ◽  
The Arctic ◽  
High Time Resolution ◽  
Data Sets ◽  
Atmospheric Ozone ◽  
Polar Day ◽  
Microwave Radiometers ◽  
Chemical Reaction Rates

Abstract. We present an analysis of the diurnal ozone cycle from 1 year of continuous ozone measurements from two ground-based microwave radiometers in the Arctic. The instruments GROMOS-C and OZORAM are located at the AWIPEV research base at Ny-Ålesund, Svalbard (79° N, 12° E), and gathered a comprehensive time series of middle-atmospheric ozone profiles with a high time resolution. An intercomparison was performed with EOS MLS and ozone sonde measurements and simulations with SD-WACCM. The measured data sets were used to study the photochemically induced diurnal cycle of ozone in the stratosphere and mesosphere. Throughout the year the insolation in the Arctic changes drastically from polar night to polar day. Accordingly, the seasonal variations in the diurnal ozone cycle are large. In the stratosphere we found a diurnal cycle throughout the entire period of polar day with the largest amplitude in April. In the mesosphere a diurnal cycle was detected in spring and fall. SD-WACCM has been proven to capture the diurnal cycle well and was therefore used to analyse the chemical reaction rates of ozone production and loss at equinox and summer solstice. Furthermore GROMOS-C proved capable of measuring the tertiary ozone layer above Ny-Ålesund in winter.

scholarly journals Investigation of Arctic middle-atmospheric dynamics using 3 years of H<sub>2</sub>O and O<sub>3</sub> measurements from microwave radiometers at Ny-Ålesund

2019 ◽  
Author(s):  
Franziska Schranz ◽  
Brigitte Tschanz ◽  
Rolf Rüfenacht ◽  
Klemens Hocke ◽  
Mathias Palm ◽  
...  
Keyword(s):  
Water Vapour ◽  
Middle Atmosphere ◽  
Microwave Radiometer ◽  
Polar Vortex ◽  
The Arctic ◽  
High Time Resolution ◽  
Middle Atmospheric Dynamics ◽  
Wind Profiles ◽  
Microwave Radiometers

Abstract. We use 3 years of water vapour and ozone measurements to analyse dynamical events in the polar middle atmosphere such as sudden stratospheric warmings (SSW), polar vortex shifts, water vapour descent rates and periodicities. The measurements were performed with the two ground-based microwave radiometers MIAWARA-C and GROMOS-C which are co-located at the AWIPEV research base at Ny-Ålesund, Svalbard (79° N, 12° E) since September 2015. The almost continuous datasets of water vapour and ozone are characterised by a high time resolution in the order of hours. A thorough intercomparison of these datasets with models and measurements from satellite, ground-based and in-situ instruments was performed. In the upper stratosphere and lower mesosphere the MIAWARA-C profiles agree within 5 % with SD-WACCM simulations and ACE-FTS measurements whereas AuraMLS measurements show an average offset of 10–15 % depending on altitude but constant in time. Stratospheric GROMOS-C profiles are within 5 % of the satellite instruments AuraMLS and ACE-FTS and the ground-based microwave radiometer OZORAM which is also located at Ny-Ålesund. During these first three years of the measurement campaign typical phenomena of the Arctic middle atmosphere took place and we analysed their signatures in the water vapour and ozone datasets. Inside of the polar vortex in autumn we found the descent rate of mesospheric water vapour to be 435 m/day on average. In early 2017 distinct increases in mesospheric water vapour of about 2 ppm were observed when the polar vortex was displaced and midlatitude air was brought to Ny-Ålesund. Two major sudden stratospheric warmings took place in March 2016 and February 2018 where ozone enhancements of up to 4 ppm were observed. The zonal wind reversals accompanying a major SSW were captured in the GROMOS-C wind profiles which are retrieved from the ozone spectra. After the SSW in February 2018 the polar vortex re-established and the water vapour descent rate in the mesosphere was 355 m/day. In the water vapour and ozone time series signatures of atmospheric waves with periods close to 2, 5, 10 and 16 days were found.

scholarly journals Investigation of Arctic middle-atmospheric dynamics using 3 years of H<sub>2</sub>O and O<sub>3</sub> measurements from microwave radiometers at Ny-Ålesund

2019 ◽  
Vol 19 (15) ◽  
pp. 9927-9947 ◽  
Author(s):  
Franziska Schranz ◽  
Brigitte Tschanz ◽  
Rolf Rüfenacht ◽  
Klemens Hocke ◽  
Mathias Palm ◽  
...  
Keyword(s):  
Water Vapour ◽  
Middle Atmosphere ◽  
Microwave Radiometer ◽  
Polar Vortex ◽  
Atmospheric Composition ◽  
The Arctic ◽  
High Time Resolution ◽  
Mean Meridional Circulation ◽  
Wind Profiles ◽  
Microwave Radiometers

Abstract. We used 3 years of water vapour and ozone measurements to study the dynamics in the Arctic middle atmosphere. We investigated the descent of water vapour within the polar vortex, major and minor sudden stratospheric warmings and periodicities at Ny-Ålesund. The measurements were performed with the two ground-based microwave radiometers MIAWARA-C and GROMOS-C, which have been co-located at the AWIPEV research base at Ny-Ålesund, Svalbard (79∘ N, 12∘ E), since September 2015. Both instruments belong to the Network for the Detection of Atmospheric Composition Change (NDACC). The almost continuous datasets of water vapour and ozone are characterized by a high time resolution of the order of hours. A thorough intercomparison of these datasets with models and measurements from satellite, ground-based and in situ instruments was performed. In the upper stratosphere and lower mesosphere the MIAWARA-C water vapour profiles agree within 5 % with SD-WACCM simulations and ACE-FTS measurements on average, whereas AuraMLS measurements show an average offset of 10 %–15 % depending on altitude but constant in time. Stratospheric GROMOS-C ozone profiles are on average within 6 % of the SD-WACCM model, the AuraMLS and ACE-FTS satellite instruments and the OZORAM ground-based microwave radiometer which is also located at Ny-Ålesund. During these first 3 years of the measurement campaign typical phenomena of the Arctic middle atmosphere took place, and we analysed their signatures in the water vapour and ozone measurements. Two major sudden stratospheric warmings (SSWs) took place in March 2016 and February 2018 and three minor warmings were observed in early 2017. Ozone-rich air was brought to the pole and during the major warmings ozone enhancements of up to 4 ppm were observed. The reversals of the zonal wind accompanying a major SSW were captured in the GROMOS-C wind profiles which are retrieved from the ozone spectra. After the SSW in February 2018 the polar vortex re-established and the water vapour descent rate in the mesosphere was 355 m d−1. Inside of the polar vortex in autumn we found the descent rate of mesospheric water vapour from MIAWARA-C to be 435 m d−1 on average. We find that the water vapour descent rate from SD-WACCM and the vertical velocity w‾* of the residual mean meridional circulation from SD-WACCM are substantially higher than the descent rates of MIAWARA-C. w‾* and the zonal mean water vapour descent rate from SD-WACCM agree within 10 % after the SSW, whereas in autumn w‾* is up to 40 % higher. We further present an overview of the periodicities in the water vapour and ozone measurements and analysed seasonal and interannual differences.

scholarly journals Analysis of the latitudinal variability of tropospheric ozone in the Arctic using the large number of aircraft and ozonesonde observations in early summer 2008

2016 ◽  
Author(s):  
Gerard Ancellet ◽  
Nikos Daskalakis ◽  
Jean Christophe Raut ◽  
Boris Quennehen ◽  
François Ravetta ◽  
...  
Keyword(s):  
Biomass Burning ◽  
Tropospheric Ozone ◽  
Lower Troposphere ◽  
Early Summer ◽  
Ozone Production ◽  
The Arctic ◽  
Integrated Analysis ◽  
International Polar Year ◽  
Latitude Range ◽  
Vertical Variability

Abstract. The goal of the paper are to: (1) present tropospheric ozone (O3) climatologies in summer 2008 based on a large amount of measurements, during the International Polar Year when the Polar Study using Aircraft, Remote Sensing, Surface Measurements, and Models of Climate Chemistry, Aerosols, and Transport (POLARCAT) campaigns were conducted (2) investigate the processes that determine O3 concentrations in two different regions (Canada and Greenland) that were thoroughly studied using measurements from 3 aircraft and 7 ozonesonde stations. This paper provides an integrated analysis of these observations and the discussion of the latitudinal and vertical variability of tropospheric ozone north of 55° N during this period is performed using a regional model (WFR-Chem). Ozone, CO and potential vorticity (PV) distributions are extracted from the simulation at the measurement locations. The model is able to reproduce the O3 latitudinal and vertical variability but a negative O3 bias of 6–15 ppbv is found in the free troposphere over 4 km, especially over Canada. Ozone average concentrations are of the order of 65 ppbv at altitudes above 4 km both over Canada and Greenland, while they are less than 50 ppbv in the lower troposphere. The relative influence of stratosphere-troposphere exchange (STE) and of ozone production related to the local biomass burning (BB) emissions is discussed using differences between average values of O3, CO and PV for Southern and Northern Canada or Greenland and two vertical ranges in the troposphere: 0–4 km and 4–8 km. For Canada, the model CO distribution and the weak correlation (< 30 %) of O3 and PV suggests that stratosphere-troposphere exchange (STE) is not the major contribution to average tropospheric ozone at latitudes less than 70° N, due to the fact that local biomass burning (BB) emissions were significant during the 2008 summer period. Conversely over Greenland, significant STE is found according to the better O3 versus PV correlation (> 40 %) and the higher 75th PV percentile. A weak negative latitudinal summer ozone gradient −6 to −8 ppbv is found over Canada in the mid troposphere between 4 and 8 km. This is attributed to an efficient O3 photochemical production due to the BB emissions at latitudes less than 65° N, while STE contribution is more homogeneous in the latitude range 55° N to 70° N. A positive ozone latitudinal gradient of 12 ppbv is observed in the same altitude range over Greenland not because of an increasing latitudinal influence of STE, but because of different long range transport from multiple mid-latitude sources (North America, Europe and even Asia for latitudes higher than 77° N).

scholarly journals The influence of temperature on ozone production under varying NO<sub><i>x</i></sub> conditions – a modelling study

2016 ◽  
Vol 16 (18) ◽  
pp. 11601-11615 ◽  
Author(s):  
Jane Coates ◽  
Kathleen A. Mar ◽  
Narendra Ojha ◽  
Tim M. Butler
Keyword(s):  
Central Europe ◽  
Surface Ozone ◽  
Reaction Rates ◽  
Air Pollutant ◽  
Box Model ◽  
Chemical Mechanism ◽  
Ozone Production ◽  
Nox Emissions ◽  
Model Simulations ◽  
Rate Of Increase

Abstract. Surface ozone is a secondary air pollutant produced during the atmospheric photochemical degradation of emitted volatile organic compounds (VOCs) in the presence of sunlight and nitrogen oxides (NOx). Temperature directly influences ozone production through speeding up the rates of chemical reactions and increasing the emissions of VOCs, such as isoprene, from vegetation. In this study, we used an idealised box model with different chemical mechanisms (Master Chemical Mechanism, MCMv3.2; Common Representative Intermediates, CRIv2; Model for OZone and Related Chemical Tracers, MOZART-4; Regional Acid Deposition Model, RADM2; Carbon Bond Mechanism, CB05) to examine the non-linear relationship between ozone, NOx and temperature, and we compared this to previous observational studies. Under high-NOx conditions, an increase in ozone from 20 to 40 °C of up to 20 ppbv was due to faster reaction rates, while increased isoprene emissions added up to a further 11 ppbv of ozone. The largest inter-mechanism differences were obtained at high temperatures and high-NOx emissions. CB05 and RADM2 simulated more NOx-sensitive chemistry than MCMv3.2, CRIv2 and MOZART-4, which could lead to different mitigation strategies being proposed depending on the chemical mechanism. The increased oxidation rate of emitted VOC with temperature controlled the rate of Ox production; the net influence of peroxy nitrates increased net Ox production per molecule of emitted VOC oxidised. The rate of increase in ozone mixing ratios with temperature from our box model simulations was about half the rate of increase in ozone with temperature observed over central Europe or simulated by a regional chemistry transport model. Modifying the box model set-up to approximate stagnant meteorological conditions increased the rate of increase of ozone with temperature as the accumulation of oxidants enhanced ozone production through the increased production of peroxy radicals from the secondary degradation of emitted VOCs. The box model simulations approximating stagnant conditions and the maximal ozone production chemical regime reproduced the 2 ppbv increase in ozone per degree Celsius from the observational and regional model data over central Europe. The simulated ozone–temperature relationship was more sensitive to mixing than the choice of chemical mechanism. Our analysis suggests that reductions in NOx emissions would be required to offset the additional ozone production due to an increase in temperature in the future.

Ignition and combustion of a hydrogen jet in air with finite chemical reaction rates

1974 ◽  
Vol 10 (1) ◽  
pp. 56-62
Author(s):  
V. K. Baev ◽  
V. I. Golovichev ◽  
V. I. Dimitrov ◽  
V. A. Yasakov
Keyword(s):  
Chemical Reaction ◽  
Reaction Rates ◽  
Ignition And Combustion ◽  
Chemical Reaction Rates

scholarly journals Numerical analysis of the chemical kinetic mechanisms of ozone depletion and halogen release in the polar troposphere

2013 ◽  
Vol 13 (9) ◽  
pp. 24171-24222 ◽  
Author(s):  
L. Cao ◽  
H. Sihler ◽  
U. Platt ◽  
E. Gutheil
Keyword(s):  
Boundary Layer ◽  
Surface Area ◽  
Ozone Depletion ◽  
Reaction Rates ◽  
The Arctic ◽  
Strong Impact ◽  
Reactive Surface ◽  
A Value ◽  
Halogen Species

Abstract. In recent years, the role of halogen species (e.g. Br, Cl) in the troposphere of polar regions is investigated after the discovery of their importance for boundary layer ozone destruction in the polar spring. Halogen species take part in an auto-catalytic chemical cycle including key self reactions. In this study, several chemical reaction schemes are investigated, and the importance of specific reactions and their rate constants is identified by a sensitivity analysis. A category of heterogeneous reactions related to HOBr activate halogen ions from sea salt aerosols, fresh sea ice or snow pack, driving the "bromine explosion". In the Arctic, a small amount of NOx may exist, which comes from nitrate contained in the snow, and this NOx may have a strong impact on ozone depletion. The heterogeneous reaction rates are parameterized by considering the aerodynamic resistance, a reactive surface ratio, β, i.e. ratio of reactive surface area to total ground surface area, and the boundary layer height, Lmix. It is found that for β = 1, the ozone depletion process starts after five days and lasts for 40 h for Lmix = 200 m. Ozone depletion duration becomes independent of the height of the boundary layer for about β≥20, and it approaches a value of two days for β=100. The role of nitrogen and chlorine containing species on the ozone depletion rate is studied. The calculation of the time integrated bromine and chlorine atom concentrations suggests a value in the order of 103 for the [Br] / [Cl] ratio, which reveals that atomic chlorine radicals have minor direct influence on the ozone depletion. The NOx concentrations are influenced by different chemical cycles over different time periods. During ozone depletion, the reaction cycle involving the BrONO2 hydrolysis is dominant. A critical value of 0.002 of the uptake coefficient of the BrONO2 hydrolysis reaction at the aerosol and saline surfaces is identified, beyond which the existence of NOx species accelerate the ozone depletion event – for lower values, deceleration occurs.

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