Introduction to special section on the Northern Wetlands Study and the Arctic Boundary Layer Expedition 3B: An international and interdisciplinary field campaign

1994 ◽  
Vol 99 (D1) ◽  
pp. 1421 ◽  
Author(s):  
Lee F. Klinger
Keyword(s):  
Boundary Layer ◽  
Special Section ◽  
The Arctic ◽  
Arctic Boundary Layer ◽  
Field Campaign ◽  
Interdisciplinary Field

scholarly journals An aircraft-borne chemical ionization – ion trap mass spectrometer (CI-ITMS) for fast PAN and PPN measurements

2010 ◽  
Vol 3 (5) ◽  
pp. 4313-4354
Author(s):  
A. Roiger ◽  
H. Aufmhoff ◽  
P. Stock ◽  
F. Arnold ◽  
H. Schlager
Keyword(s):  
Boundary Layer ◽  
Mass Spectrometer ◽  
Chemical Ionization ◽  
Ion Trap ◽  
The Arctic ◽  
Arctic Boundary Layer ◽  
Online Calibration ◽  
Mixing Ratios ◽  
Ion Trap Mass Spectrometer ◽  
Research Aircraft

Abstract. An airborne chemical ionization ion trap mass spectrometer instrument (CI-ITMS) has been developed for tropospheric and stratospheric fast in-situ measurements of PAN (peroxyacetyl nitrate) and PPN (peroxypropionyl nitrate). The first scientific deployment of the FASTPEX instrument (FASTPEX = Fast Measurement of Peroxyacyl nitrates) took place in the Arctic during 18 missions aboard the DLR research aircraft Falcon, within the framework of the POLARCAT-GRACE campaign in the summer of 2008. The FASTPEX instrument is described and characteristic properties of the employed ion trap mass spectrometer are discussed. Atmospheric data obtained at altitudes of up to ~12 km are presented, from the boundary layer to the lowermost stratosphere. Data were sampled with a time resolution of 2 s and a 2σ detection limit of 25 pmol mol−1. An isotopically labelled standard was used for a permanent online calibration. For this reason the accuracy of the PAN measurements is better than ±10% for mixing ratios greater than 200 pmol mol−1. PAN mixing ratios in the summer Arctic troposphere were in the order of a few hundred pmol mol−1 and generally correlated well with CO. In the Arctic boundary layer and lowermost stratosphere smaller PAN mixing ratios were observed due to a combination of missing local sources of PAN precursor gases and efficient removal processes (thermolysis/photolysis). PPN, the second most abundant PAN homologue, was measured simultanously. Observed PPN/PAN ratios range between ~0.03 and 0.3.

scholarly journals The Arctic Boundary Layer Expedition (ABLE 3A): July–August 1988

1992 ◽  
Vol 97 (D15) ◽  
pp. 16383 ◽  
Author(s):  
R. C. Harriss ◽  
S. C. Wofsy ◽  
D. S. Bartlett ◽  
M. C. Shipham ◽  
D. J. Jacob ◽  
...  
Keyword(s):  
Boundary Layer ◽  
The Arctic ◽  
Arctic Boundary Layer

scholarly journals Ozone variability and halogen oxidation within the Arctic and sub-Arctic springtime boundary layer

2010 ◽  
Vol 10 (21) ◽  
pp. 10223-10236 ◽  
Author(s):  
J. B. Gilman ◽  
J. F. Burkhart ◽  
B. M. Lerner ◽  
E. J. Williams ◽  
W. C. Kuster ◽  
...  
Keyword(s):  
Boundary Layer ◽  
North Atlantic ◽  
Marine Boundary Layer ◽  
Transport Model ◽  
Arctic Basin ◽  
The Arctic ◽  
Arctic Boundary Layer ◽  
Air Masses ◽  
The North ◽  
The North Atlantic

Abstract. The influence of halogen oxidation on the variabilities of ozone (O3) and volatile organic compounds (VOCs) within the Arctic and sub-Arctic atmospheric boundary layer was investigated using field measurements from multiple campaigns conducted in March and April 2008 as part of the POLARCAT project. For the ship-based measurements, a high degree of correlation (r = 0.98 for 544 data points collected north of 68° N) was observed between the acetylene to benzene ratio, used as a marker for chlorine and bromine oxidation, and O3 signifying the vast influence of halogen oxidation throughout the ice-free regions of the North Atlantic. Concurrent airborne and ground-based measurements in the Alaskan Arctic substantiated this correlation and were used to demonstrate that halogen oxidation influenced O3 variability throughout the Arctic boundary layer during these springtime studies. Measurements aboard the R/V Knorr in the North Atlantic and Arctic Oceans provided a unique view of the transport of O3-poor air masses from the Arctic Basin to latitudes as far south as 52° N. FLEXPART, a Lagrangian transport model, was used to quantitatively determine the exposure of air masses encountered by the ship to first-year ice (FYI), multi-year ice (MYI), and total ICE (FYI+MYI). O3 anti-correlated with the modeled total ICE tracer (r = −0.86) indicating that up to 73% of the O3 variability measured in the Arctic marine boundary layer could be related to sea ice exposure.

scholarly journals Signature of Arctic surface ozone depletion events in the isotope anomaly (Δ<sup>17</sup>O) of atmospheric nitrate

2007 ◽  
Vol 7 (5) ◽  
pp. 1451-1469 ◽  
Author(s):  
S. Morin ◽  
J. Savarino ◽  
S. Bekki ◽  
S. Gong ◽  
J. W. Bottenheim
Keyword(s):  
Boundary Layer ◽  
Ozone Depletion ◽  
Surface Ozone ◽  
The Arctic ◽  
Arctic Boundary Layer ◽  
Mixing Ratios ◽  
Atmospheric Nitrate ◽  
Boundary Layer Ozone ◽  
Oxidation Of No ◽  
Arctic Surface

Abstract. We report the first measurements of the oxygen isotope anomaly of atmospheric inorganic nitrate from the Arctic. Nitrate samples and complementary data were collected at Alert, Nunavut, Canada (82°30 ' N, 62°19 ' W) in spring 2004. Covering the polar sunrise period, characterized by the occurrence of severe boundary layer ozone depletion events (ODEs), our data show a significant correlation between the variations of atmospheric ozone (O3) mixing ratios and Δ17O of nitrate (Δ17O(NO−3)). This relationship can be expressed as: Δ17O(NO−3)/‰, =(0.15±0.03)×O3/(nmol mol–1)+(29.7±0.7), with R2=0.70(n=12), for Δ17O(NO−3) ranging between 29 and 35 ‰. We derive mass-balance equations from chemical reactions operating in the Arctic boundary layer, that describe the evolution of Δ17O(NO−3) as a function of the concentrations of reactive species and their isotopic characteristics. Changes in the relative importance of O3, RO2 and BrO in the oxidation of NO during ODEs, and the large isotope anomalies of O3 and BrO, are the driving force for the variability in the measured Δ17O(NO−3) . BrONO2 hydrolysis is found to be a dominant source of nitrate in the Arctic boundary layer, in agreement with recent modeling studies.

scholarly journals Analysis of reactive bromine production and ozone depletion in the Arctic boundary layer using 3-D simulations with GEM-AQ: inference from synoptic-scale patterns

2011 ◽  
Vol 11 (8) ◽  
pp. 3949-3979 ◽  
Author(s):  
K. Toyota ◽  
J. C. McConnell ◽  
A. Lupu ◽  
L. Neary ◽  
C. A. McLinden ◽  
...  
Keyword(s):  
Boundary Layer ◽  
Sea Ice ◽  
Ozone Depletion ◽  
Surface Ozone ◽  
High Arctic ◽  
Heterogeneous Reactions ◽  
The Arctic ◽  
Synoptic Scale ◽  
Arctic Boundary Layer ◽  
Surface Snow

Abstract. Episodes of high bromine levels and surface ozone depletion in the springtime Arctic are simulated by an online air-quality model, GEM-AQ, with gas-phase and heterogeneous reactions of inorganic bromine species and a simple scheme of air-snowpack chemical interactions implemented for this study. Snowpack on sea ice is assumed to be the only source of bromine to the atmosphere and to be capable of converting relatively stable bromine species to photolabile Br2 via air-snowpack interactions. A set of sensitivity model runs are performed for April 2001 at a horizontal resolution of approximately 100 km×100 km in the Arctic, to provide insights into the effects of temperature and the age (first-year, FY, versus multi-year, MY) of sea ice on the release of reactive bromine to the atmosphere. The model simulations capture much of the temporal variations in surface ozone mixing ratios as observed at stations in the high Arctic and the synoptic-scale evolution of areas with enhanced BrO column amount ("BrO clouds") as estimated from satellite observations. The simulated "BrO clouds" are in modestly better agreement with the satellite measurements when the FY sea ice is assumed to be more efficient at releasing reactive bromine to the atmosphere than on the MY sea ice. Surface ozone data from coastal stations used in this study are not sufficient to evaluate unambiguously the difference between the FY sea ice and the MY sea ice as a source of bromine. The results strongly suggest that reactive bromine is released ubiquitously from the snow on the sea ice during the Arctic spring while the timing and location of the bromine release are largely controlled by meteorological factors. It appears that a rapid advection and an enhanced turbulent diffusion associated with strong boundary-layer winds drive transport and dispersion of ozone to the near-surface air over the sea ice, increasing the oxidation rate of bromide (Br−) in the surface snow. Also, if indeed the surface snowpack does supply most of the reactive bromine in the Arctic boundary layer, it appears to be capable of releasing reactive bromine at temperatures as high as −10 °C, particularly on the sea ice in the central and eastern Arctic Ocean. Dynamically-induced BrO column variability in the lowermost stratosphere appears to interfere with the use of satellite BrO column measurements for interpreting BrO variability in the lower troposphere but probably not to the extent of totally obscuring "BrO clouds" that originate from the surface snow/ice source of bromine in the high Arctic. A budget analysis of the simulated air-surface exchange of bromine compounds suggests that a "bromine explosion" occurs in the interstitial air of the snowpack and/or is accelerated by heterogeneous reactions on the surface of wind-blown snow in ambient air, both of which are not represented explicitly in our simple model but could have been approximated by a parameter adjustment for the yield of Br2 from the trigger.

scholarly journals NYTEFOX – The NY-Ålesund TurbulencE Fiber Optic eXperiment investigating the Arctic boundary layer, Svalbard

2021 ◽  
Author(s):  
Marie-Louise Zeller ◽  
Jannis-Michael Huss ◽  
Lena Pfister ◽  
Karl E. Lapo ◽  
Daniela Littmann ◽  
...  
Keyword(s):  
Boundary Layer ◽  
Field Experiment ◽  
Fiber Optic ◽  
Meteorological Data ◽  
Surface Radiation ◽  
The Arctic ◽  
Vertical Profiles ◽  
Arctic Boundary Layer ◽  
Data Set ◽  
Sonic Anemometers

Abstract. The NY-Ålesund TurbulencE Fiber Optic eXperiment, NYTEFOX, was a field experiment at the Arctic site Ny-Ålesund (11.9° E, 78.9° N) and yielded a unique meteorological data set. These data describe the distribution of heat, airflows, and exchange in the Arctic boundary layer for a period of 14 days from 26 February to 10 March 2020. NYTEFOX is the first field experiment to investigate the heterogeneity of airflow and its transport in temperatures, wind, and kinetic energy in the Arctic environment using the Fiber-Optic Distributed Sensing (FODS) technique for horizontal and vertical observations. FODS air temperature and wind speed were observed at a spatial resolution of 0.127 m and 9 s in time along a horizontal array of 700 m at 1 m height above ground level (agl) and along three 7 m vertical profiles. Ancillary data were collected from three sonic anemometers and an acoustic profiler (miniSodar, SOund Detection And Ranging) yielding turbulent flow statistics and vertical profiles in the lowest 300 m agl, respectively. The observations from this field campaign are publicly available on Zenodo (https://doi.org/10.5281/zenodo.4335461) and supplement the data set operationally collected by the Basic Surface Radiation Network (BSRN) meteorological data set at Ny-Ålesund, Svalbard.

scholarly journals Chemical composition and source attribution of submicron aerosol particles in the summertime Arctic lower troposphere

2020 ◽  
Author(s):  
Franziska Köllner ◽  
Johannes Schneider ◽  
Megan D. Willis ◽  
Hannes Schulz ◽  
Daniel Kunkel ◽  
...  
Keyword(s):  
Boundary Layer ◽  
Organic Matter ◽  
Elemental Carbon ◽  
Dicarboxylic Acids ◽  
The Arctic ◽  
Arctic Boundary Layer ◽  
Air Mass ◽  
Particle Composition ◽  
Arctic Regions ◽  
Vegetation Fires

Abstract. We use airborne measurements of aerosol particle composition to demonstrate the strong contrast between particle sources and composition within and above the summertime Arctic boundary layer. In-situ measurements from two complementary aerosol mass spectrometers, the ALABAMA and the HR-ToF-AMS, with black carbon measurements from an SP2 are presented. Particle composition analysis was complemented by trace gas measurements, satellite data, and air mass history modeling to attribute particle properties to particle origin and air mass source regions. Particle composition above the summertime Arctic boundary layer was dominated by chemically aged particles, containing elemental carbon, nitrate, ammonium, sulfate, and organic matter. From our analysis, we conclude that the presence of these particles was driven by transport of aerosol and precursor gases from mid-latitudes to Arctic regions. Particularly, elevated concentrations of nitrate, ammonium, and organic matter coincided with time spent over vegetation fires in northern Canada. In parallel, those particles were largely present in high CO environments (> 90 ppbv). Additionally, we observed that the organic-to-sulfate ratio was enhanced with increasing influence from these fires. Besides vegetation fires, particle sources in mid-latitudes further include anthropogenic emissions in Europe, North America, and East Asia. The presence of particles in the Arctic lower free troposphere correlated with time spent over populated and industrial areas in these regions. Further, the size distribution of free tropospheric particles containing elemental carbon and nitrate was shifter to larger diameters compared to particles present within the boundary layer. Moreover, our analysis suggests that organic matter when present in the Arctic free troposphere can partly be identified as low-molecular weight dicarboxylic acids (oxalic, malonic, and succinic acid). Particles containing dicarboxylic acids were largely present when the residence time of air masses outside Arctic regions was high. In contrast, particle composition within the marine boundary layer was largely driven by Arctic regional processes. Air mass history modeling demonstrated that alongside primary sea spray particles, marine-biogenic sources contributed to secondary aerosol formation by trimethylamine, methanesulfonic acid, sulfate, and other organic species.

scholarly journals The NY-Ålesund TurbulencE Fiber Optic eXperiment (NYTEFOX): investigating the Arctic boundary layer, Svalbard

2021 ◽  
Vol 13 (7) ◽  
pp. 3439-3452
Author(s):  
Marie-Louise Zeller ◽  
Jannis-Michael Huss ◽  
Lena Pfister ◽  
Karl E. Lapo ◽  
Daniela Littmann ◽  
...  
Keyword(s):  
Boundary Layer ◽  
Field Experiment ◽  
Fiber Optic ◽  
Meteorological Data ◽  
Surface Radiation ◽  
The Arctic ◽  
Vertical Profiles ◽  
Arctic Boundary Layer ◽  
Data Set ◽  
Sonic Anemometers

Abstract. The NY-Ålesund TurbulencE Fiber Optic eXperiment (NYTEFOX) was a field experiment at the Ny-Ålesund Arctic site (78.9∘ N, 11.9∘ E) and yielded a unique meteorological data set. These data describe the distribution of heat, airflows, and exchange in the Arctic boundary layer for a period of 14 d from 26 February to 10 March 2020. NYTEFOX is the first field experiment to investigate the heterogeneity of airflow and its transport of temperature, wind, and kinetic energy in the Arctic environment using the fiber-optic distributed sensing (FODS) technique for horizontal and vertical observations. FODS air temperature and wind speed were observed at a spatial resolution of 0.127 m and a temporal resolution of 9 s along a 700 m horizontal array at 1 m above ground level (a.g.l.) and along three 7 m vertical profiles. Ancillary data were collected from three sonic anemometers and an acoustic profiler (minisodar; sodar is an acronym for “sound detection and ranging”) yielding turbulent flow statistics and vertical profiles in the lowest 300 m a.g.l., respectively. The observations from this field campaign are publicly available on Zenodo (https://doi.org/10.5281/zenodo.4756836, Huss et al., 2021) and supplement the meteorological data set operationally collected by the Baseline Surface Radiation Network (BSRN) at Ny-Ålesund, Svalbard.

Alkenes in the Arctic boundary layer at Alert, Nunavut, Canada

2002 ◽  
Vol 36 (15-16) ◽  
pp. 2585-2594 ◽  
Author(s):  
Jan W Bottenheim ◽  
Hacene Boudries ◽  
Peter C Brickell ◽  
Elliot Atlas
Keyword(s):  
Boundary Layer ◽  
The Arctic ◽  
Arctic Boundary Layer

scholarly journals An aircraft-borne chemical ionization – ion trap mass spectrometer (CI-ITMS) for fast PAN and PPN measurements

2011 ◽  
Vol 4 (2) ◽  
pp. 173-188 ◽  
Author(s):  
A. Roiger ◽  
H. Aufmhoff ◽  
P. Stock ◽  
F. Arnold ◽  
H. Schlager
Keyword(s):  
Boundary Layer ◽  
Mass Spectrometer ◽  
Chemical Ionization ◽  
Ion Trap ◽  
The Arctic ◽  
Arctic Boundary Layer ◽  
Mixing Ratios ◽  
Ion Trap Mass Spectrometer ◽  
Research Aircraft ◽  
On Line

Abstract. An airborne chemical ionization ion trap mass spectrometer instrument (CI-ITMS) has been developed for tropospheric and stratospheric fast in-situ measurements of PAN (peroxyacetyl nitrate) and PPN (peroxypropionyl nitrate). The first scientific deployment of the FASTPEX instrument (FASTPEX = Fast Measurement of Peroxyacyl nitrates) took place in the Arctic during 18 missions aboard the DLR research aircraft Falcon, within the framework of the POLARCAT-GRACE campaign in the summer of 2008. The FASTPEX instrument is described and characteristic properties of the employed ion trap mass spectrometer are discussed. Atmospheric data obtained at altitudes of up to ~12 km are presented, from the boundary layer to the lowermost stratosphere. Data were sampled with a time resolution of 2 s and a 2σ detection limit of 25 pmol mol−1. An isotopically labelled standard was used for a permanent on-line calibration. For this reason the accuracy of the PAN measurements is better than ±10% for mixing ratios greater than 200 pmol mol−1. PAN mixing ratios in the summer Arctic troposphere were in the order of a few hundred pmol mol−1 and generally correlated well with CO. In the Arctic boundary layer and lowermost stratosphere smaller PAN mixing ratios were observed due to a combination of missing local sources of PAN precursor gases and efficient removal processes (thermolysis/photolysis). PPN, the second most abundant PAN homologue, was measured simultaneously. Observed PPN/PAN ratios range between ~0.03 and 0.3.

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