The total hydrogen budget in the Arctic winter stratosphere during the European Arctic Stratospheric Ozone Experiment

1996 ◽  
Vol 101 (D9) ◽  
pp. 14495-14503 ◽  
Author(s):  
Andreas Engel ◽  
Cornelius Schiller ◽  
Ulrich Schmidt ◽  
Reinhard Borchers ◽  
Henry Ovarlez ◽  
...  
Keyword(s):  
Stratospheric Ozone ◽  
The Arctic ◽  
European Arctic ◽  
Ozone Experiment

Airborne measurements during the European Arctic Stratospheric Ozone Experiment: Observation of OClO

1994 ◽  
Vol 21 (13) ◽  
pp. 1363-1366 ◽  
Author(s):  
Ronald Brandtjen ◽  
T. Klüpfel ◽  
D. Perner ◽  
B. M. Knudsen
Keyword(s):  
Stratospheric Ozone ◽  
Airborne Measurements ◽  
European Arctic ◽  
Ozone Experiment

scholarly journals The Diurnal Variation in Stratospheric Ozone from MACC Reanalysis, ERA-Interim, WACCM, and Earth Observation Data: Characteristics and Intercomparison

Atmosphere ◽  
2021 ◽  
Vol 12 (5) ◽  
pp. 625
Author(s):  
Ansgar Schanz ◽  
Klemens Hocke ◽  
Niklaus Kämpfer ◽  
Simon Chabrillat ◽  
Antje Inness ◽  
...  
Keyword(s):  
Diurnal Variation ◽  
Climate Model ◽  
Stratospheric Ozone ◽  
Polar Vortex ◽  
Model Systems ◽  
Atmospheric Composition ◽  
The Arctic ◽  
Observation Data ◽  
High Latitudes ◽  
Free Running

In this study, we compare the diurnal variation in stratospheric ozone of the MACC (Monitoring Atmospheric Composition and Climate) reanalysis, ECMWF Reanalysis Interim (ERA-Interim), and the free-running WACCM (Whole Atmosphere Community Climate Model). The diurnal variation of stratospheric ozone results from photochemical and dynamical processes depending on altitude, latitude, and season. MACC reanalysis and WACCM use similar chemistry modules and calculate a similar diurnal cycle in ozone when it is caused by a photochemical variation. The results of the two model systems are confirmed by observations of the Superconducting Submillimeter-Wave Limb-Emission Sounder (SMILES) experiment and three selected sites of the Network for Detection of Atmospheric Composition Change (NDACC) at Mauna Loa, Hawaii (tropics), Bern, Switzerland (midlatitudes), and Ny-Ålesund, Svalbard (high latitudes). On the other hand, the ozone product of ERA-Interim shows considerably less diurnal variation due to photochemical variations. The global maxima of diurnal variation occur at high latitudes in summer, e.g., near the Arctic NDACC site at Ny-Ålesund, Svalbard. The local OZORAM radiometer observes this effect in good agreement with MACC reanalysis and WACCM. The sensed diurnal variation at Ny-Ålesund is up to 8% (0.4 ppmv) due to photochemical variations in summer and negligible during the dynamically dominated winter. However, when dynamics play a major role for the diurnal ozone variation as in the lower stratosphere (100–20 hPa), the reanalysis models ERA-Interim and MACC which assimilate data from radiosondes and satellites outperform the free-running WACCM. Such a domain is the Antarctic polar winter where a surprising novel feature of diurnal variation is indicated by MACC reanalysis and ERA-Interim at the edge of the polar vortex. This effect accounts for up to 8% (0.4 ppmv) in both model systems. In summary, MACC reanalysis provides a global description of the diurnal variation of stratospheric ozone caused by dynamics and photochemical variations. This is of high interest for ozone trend analysis and other research which is based on merged satellite data or measurements at different local time.

Record springtime stratospheric ozone depletion at 80°N in 2020

2021 ◽  
Author(s):  
Ramina Alwarda ◽  
Kristof Bognar ◽  
Kimberly Strong ◽  
Martyn Chipperfield ◽  
Sandip Dhomse ◽  
...  
Keyword(s):  
Ozone Depletion ◽  
Transport Model ◽  
Stratospheric Ozone ◽  
Polar Vortex ◽  
The Arctic ◽  
Optical Absorption Spectroscopy ◽  
Chemical Transport Model ◽  
Polar Stratospheric Clouds ◽  
Ozone Loss ◽  
Stratospheric Clouds

<p>The Arctic winter of 2019-2020 was characterized by an unusually persistent polar vortex and temperatures in the lower stratosphere that were consistently below the threshold for the formation of polar stratospheric clouds (PSCs). These conditions led to ozone loss that is comparable to the Antarctic ozone hole. Ground-based measurements from a suite of instruments at the Polar Environment Atmospheric Research Laboratory (PEARL) in Eureka, Canada (80.05°N, 86.42°W) were used to investigate chemical ozone depletion. The vortex was located above Eureka longer than in any previous year in the 20-year dataset and lidar measurements provided evidence of polar stratospheric clouds (PSCs) above Eureka. Additionally, UV-visible zenith-sky Differential Optical Absorption Spectroscopy (DOAS) measurements showed record ozone loss in the 20-year dataset, evidence of denitrification along with the slowest increase of NO<sub>2</sub> during spring, as well as enhanced reactive halogen species (OClO and BrO). Complementary measurements of HCl and ClONO<sub>2</sub> (chlorine reservoir species) from a Fourier transform infrared (FTIR) spectrometer showed unusually low columns that were comparable to 2011, the previous year with significant chemical ozone depletion. Record low values of HNO<sub>3</sub> in the FTIR dataset are in accordance with the evidence of PSCs and a denitrified atmosphere. Estimates of chemical ozone loss were derived using passive ozone from the SLIMCAT offline chemical transport model to account for dynamical contributions to the stratospheric ozone budget.</p>

scholarly journals Denitrification, dehydration and ozone loss during the Arctic winter 2015/2016

2017 ◽  
Author(s):  
Farahnaz Khosrawi ◽  
Oliver Kirner ◽  
Björn-Martin Sinnhuber ◽  
Sören Johansson ◽  
Michael Höpfner ◽  
...  
Keyword(s):  
Atmospheric Chemistry ◽  
Stratospheric Ozone ◽  
Satellite Observations ◽  
The Arctic ◽  
Cold Pool ◽  
Polar Stratospheric Clouds ◽  
Airborne Measurements ◽  
Ozone Loss ◽  
Polar Stratosphere ◽  
Stratospheric Clouds

Abstract. The Arctic winter 2015/2016 was one of the coldest stratospheric winters in recent years. A stable vortex formed by early December and the early winter was exceptionally cold. Cold pool temperatures dropped below the Nitric Acid Trihydrate (NAT) existence temperature of about 195 K, thus allowing Polar Stratospheric Clouds (PSCs) to form. The low temperatures in the polar stratosphere persisted until early March allowing chlorine activation and catalytic ozone destruction. Satellite observations indicate that sedimentation of PSC particles led to denitrification as well as dehydration of stratospheric layers. Model simulations of the Arctic winter 2015/2016 nudged toward European Center for Medium-Range Weather Forecasts (ECMWF) analyses data were performed with the atmospheric chemistry–climate model ECHAM5/MESSy Atmospheric Chemistry (EMAC) for the Polar Stratosphere in a Changing Climate (POLSTRACC) campaign. POLSTRACC is a High Altitude and LOng Range Research Aircraft (HALO) mission aimed at the investigation of the structure, composition and evolution of the Arctic Upper Troposphere and Lower Stratosphere (UTLS). The chemical and physical processes involved in Arctic stratospheric ozone depletion, transport and mixing processes in the UTLS at high latitudes, polar stratospheric clouds as well as cirrus clouds are investigated. In this study an overview of the chemistry and dynamics of the Arctic winter 2015/2016 as simulated with EMAC is given. Further, chemical-dynamical processes such as denitrification, dehydration and ozone loss during the Arctic winter 2015/2016 are investigated. Comparisons to satellite observations by the Aura Microwave Limb Sounder (Aura/MLS) as well as to airborne measurements with the Gimballed Limb Observer for Radiance Imaging of the Atmosphere (GLORIA) performed on board of HALO during the POLSTRACC campaign show that the EMAC simulations are in fairly good agreement with observations. We derive a maximum polar stratospheric O3 loss of ~ 2 ppmv or 100 DU in terms of column in mid March. The stratosphere was denitrified by about 8 ppbv HNO3 and dehydrated by about 1 ppmv H2O in mid to end of February. While ozone loss was quite strong, but not as strong as in 2010/2011, denitrification and dehydration were so far the strongest observed in the Arctic stratosphere in the at least past 10 years.

scholarly journals Seasonal patterns in Arctic planktonic metabolism (Fram Strait – Svalbard region)

2013 ◽  
Vol 10 (3) ◽  
pp. 1451-1469 ◽  
Author(s):  
R. Vaquer-Sunyer ◽  
C. M. Duarte ◽  
J. Holding ◽  
A. Regaudie-de-Gioux ◽  
L. S. García-Corral ◽  
...  
Keyword(s):  
Arctic Ocean ◽  
Early Spring ◽  
The Arctic ◽  
Fram Strait ◽  
Metabolic Rates ◽  
Net Community Production ◽  
Western Sector ◽  
The Arctic Ocean ◽  
European Arctic ◽  
Community Production

Abstract. The metabolism of the Arctic Ocean is marked by extremely pronounced seasonality and spatial heterogeneity associated with light conditions, ice cover, water masses and nutrient availability. Here we report the marine planktonic metabolic rates (net community production, gross primary production and community respiration) along three different seasons of the year, for a total of eight cruises along the western sector of the European Arctic (Fram Strait – Svalbard region) in the Arctic Ocean margin: one at the end of 2006 (fall/winter), two in 2007 (early spring and summer), two in 2008 (early spring and summer), one in 2009 (late spring–early summer), one in 2010 (spring) and one in 2011 (spring). The results show that the metabolism of the western sector of the European Arctic varies throughout the year, depending mostly on the stage of bloom and water temperature. Here we report metabolic rates for the different periods, including the spring bloom, summer and the dark period, increasing considerably the empirical basis of metabolic rates in the Arctic Ocean, and especially in the European Arctic corridor. Additionally, a rough annual metabolic estimate for this area of the Arctic Ocean was calculated, resulting in a net community production of 108 g C m−2 yr−1.

scholarly journals The importance of Asia as a source of black carbon to the European Arctic during springtime 2013

2015 ◽  
Vol 15 (20) ◽  
pp. 11537-11555 ◽  
Author(s):  
D. Liu ◽  
B. Quennehen ◽  
E. Darbyshire ◽  
J. D. Allan ◽  
P. I. Williams ◽  
...  
Keyword(s):  
Black Carbon ◽  
Arctic Sea Ice ◽  
Anthropogenic Sources ◽  
The Arctic ◽  
Geometric Standard Deviation ◽  
Free Troposphere ◽  
Aerosol Composition ◽  
Upper Troposphere ◽  
European Arctic ◽  
Mean Concentration

Abstract. Black carbon aerosol (BC) deposited to the Arctic sea ice or present in the free troposphere can significantly affect the Earth's radiation budget at high latitudes yet the BC burden in these regions and the regional source contributions are poorly constrained. Aircraft measurements of aerosol composition in the European Arctic were conducted during the Aerosol–Cloud Coupling And Climate Interactions in the Arctic (ACCACIA) campaign in March 2013. Pollutant plumes were encountered throughout the lower to upper Arctic troposphere featuring enhancements in CO and aerosol mass loadings, which were chemically speciated into BC and non-refractory sulphate and organic matter. FLEXPART-WRF simulations have been performed to evaluate the likely contribution to the pollutants from regional ground sources. By combining up-to-date anthropogenic and open fire biomass burning (OBB) inventories, we have been able to compare the contributions made to the observed pollution layers from the sources of eastern/northern Asia (AS), Europe (EU) and North America (NA). Over 90 % of the contribution to the BC was shown to arise from non-OBB anthropogenic sources. AS sources were found to be the major contributor to the BC burden, increasing background BC loadings by a factor of 3–5 to 100.8 ± 48.4 ng sm−3 (in standard air m3 at 273.15 K and 1013.25 mbar) and 55.8 ± 22.4 ng sm−3 in the middle and upper troposphere respectively. AS plumes close to the tropopause (about 7.5–8 km) were also observed, with BC concentrations ranging from 55 to 73 ng sm−3, which will potentially have a significant radiative impact. EU sources influenced the middle troposphere with a BC mean concentration of 70.8 ± 39.1 ng sm−3 but made a minor contribution to the upper troposphere due to the relatively high latitude of the source region. The contribution of NA was shown to be much lower at all altitudes with BC mean concentration of 20 ng sm−3. The BC transported to the Arctic is mixed with a non-BC volume fraction representing between 90–95 % of the mass, and has a relatively uniform core size distribution with mass median diameter 190–210 nm and geometric standard deviation σg = 1.55–1.65 and this varied little across all source regions. It is estimated that 60–95 % of BC is scavenged between emission and receptor based on BC / ΔCO comparisons between source inventories and measurement. We show that during the springtime of 2013, the anthropogenic pollution particularly from sources in Asia, contributed significantly to BC across the European Arctic free troposphere. In contrast to previous studies, the contribution from open wildfires was minimal. Given that Asian pollution is likely to continue to rise over the coming years, it is likely that the radiative forcing in the Arctic will also continue to increase.

scholarly journals Spectral albedo of seasonal snow during intensive melt period at Sodankylä, beyond the Arctic Circle

2013 ◽  
Vol 13 (7) ◽  
pp. 3793-3810 ◽  
Author(s):  
O. Meinander ◽  
S. Kazadzis ◽  
A. Arola ◽  
A. Riihelä ◽  
P. Räisänen ◽  
...  
Keyword(s):  
Spectral Irradiance ◽  
The Arctic ◽  
Visible Range ◽  
Air Masses ◽  
Clear Sky ◽  
Effective Grain Size ◽  
European Arctic ◽  
Small Absorption ◽  
High Concentrations ◽  
Double Monochromator

Abstract. We have measured spectral albedo, as well as ancillary parameters, of seasonal European Arctic snow at Sodankylä, Finland (67°22' N, 26°39' E). The springtime intensive melt period was observed during the Snow Reflectance Transition Experiment (SNORTEX) in April 2009. The upwelling and downwelling spectral irradiance, measured at 290–550 nm with a double monochromator spectroradiometer, revealed albedo values of ~0.5–0.7 for the ultraviolet and visible range, both under clear sky and variable cloudiness. During the most intensive snowmelt period of four days, albedo decreased from 0.65 to 0.45 at 330 nm, and from 0.72 to 0.53 at 450 nm. In the literature, the UV and VIS albedo for clean snow are ~0.97–0.99, consistent with the extremely small absorption coefficient of ice in this spectral region. Our low albedo values were supported by two independent simultaneous broadband albedo measurements, and simulated albedo data. We explain the low albedo values to be due to (i) large snow grain sizes up to ~3 mm in diameter; (ii) meltwater surrounding the grains and increasing the effective grain size; (iii) absorption caused by impurities in the snow, with concentration of elemental carbon (black carbon) in snow of 87 ppb, and organic carbon 2894 ppb, at the time of albedo measurements. The high concentrations of carbon, detected by the thermal–optical method, were due to air masses originating from the Kola Peninsula, Russia, where mining and refining industries are located.

scholarly journals Effect of gas-transfer-velocity parameterization choice on CO<sub>2</sub> air–sea fluxes in the North Atlantic and European Arctic

2015 ◽  
Vol 12 (6) ◽  
pp. 2591-2616
Author(s):  
I. Wróbel ◽  
J. Piskozub
Keyword(s):  
North Atlantic ◽  
World Ocean ◽  
Software Tool ◽  
The Arctic ◽  
Gas Transfer ◽  
Transfer Velocity ◽  
Gas Transfer Velocity ◽  
The North ◽  
European Arctic ◽  
The North Atlantic

Abstract. The ocean sink is an important part of the anthropogenic CO2 budget. Because the terrestrial biosphere is usually treated as a residual, understanding the uncertainties the net flux into the ocean sink is crucial for understanding the global carbon cycle. One of the sources of uncertainty is the parameterization of CO2 gas transfer velocity. We used a recently developed software tool, FluxEngine, to calculate monthly net carbon air–sea flux for the extratropical North Atlantic, European Arctic as well as global values (or comparison) using several available parameterizations of gas transfer velocity of different dependence of wind speed, both quadratic and cubic. The aim of the study is to constrain the uncertainty caused by the choice of parameterization in the North Atlantic, a large sink of CO2 and a region with good measurement coverage, characterized by strong winds. We show that this uncertainty is smaller in the North Atlantic and in the Arctic than globally, within 5 % in the North Atlantic and 4 % in the European Arctic, comparing to 9 % for the World Ocean when restricted to functions with quadratic wind dependence and respectively 42, 40 and 67 % for all studied parameterizations. We propose an explanation of this smaller uncertainty due to the combination of higher than global average wind speeds in the North Atlantic and lack of seasonal changes in the flux direction in most of the region. We also compare the available pCO2 climatologies (Takahashi and SOCAT) pCO2 discrepancy in annual flux values of 8 % in the North Atlantic and 19 % in the European Arctic. The seasonal flux changes in the Arctic have inverse seasonal change in both climatologies, caused most probably by insufficient data coverage, especially in winter.

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