New insights in sources of the sub-micrometre aerosol at Mt. Zeppelin observatory (Spitsbergen) in the year 2015

In order to evaluate the potential impact of the Arctic anthropogenic emission sources it is essential to understand better the natural aerosol sources of the inner Arctic and the atmospheric processing of the aerosols during their transport in the Arctic atmosphere. A 1-year time series of chemical...

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Main Authors: Matthias Karl, Caroline Leck, Farshid Mashayekhy Rad, Are Bäcklund, Susana Lopez-Aparicio, Jost Heintzenberg
Format: Article
Language:English
Published: Taylor & Francis Group 2019-01-01
Series:Tellus: Series B, Chemical and Physical Meteorology
Subjects:
Online Access:http://dx.doi.org/10.1080/16000889.2019.1613143
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spelling doaj-86d24b150ef04ad2a6f3a4addad387d42020-11-25T02:57:33ZengTaylor & Francis GroupTellus: Series B, Chemical and Physical Meteorology1600-08892019-01-0171110.1080/16000889.2019.16131431613143New insights in sources of the sub-micrometre aerosol at Mt. Zeppelin observatory (Spitsbergen) in the year 2015Matthias Karl0Caroline Leck1Farshid Mashayekhy Rad2Are Bäcklund3Susana Lopez-Aparicio4Jost Heintzenberg5Helmholtz-Zentrum GeesthachtStockholm UniversityStockholm UniversityNILU, Norwegian Institute for Air ResearchNILU, Norwegian Institute for Air ResearchLeibniz-Institute for Tropospheric ResearchIn order to evaluate the potential impact of the Arctic anthropogenic emission sources it is essential to understand better the natural aerosol sources of the inner Arctic and the atmospheric processing of the aerosols during their transport in the Arctic atmosphere. A 1-year time series of chemically specific measurements of the sub-micrometre aerosol during 2015 has been taken at the Mt. Zeppelin observatory in the European Arctic. A source apportionment study combined measured molecular tracers as source markers, positive matrix factorization, analysis of the potential source distribution and auxiliary information from satellite data and ground-based observations. The annual average sub-micrometre mass was apportioned to regional background secondary sulphate (56%), sea spray (17%), biomass burning (15%), secondary nitrate (5.8%), secondary marine biogenic (4.5%), mixed combustion (1.6%), and two types of marine gel sources (together 0.7%). Secondary nitrate aerosol mainly contributed towards the end of summer and during autumn. During spring and summer, the secondary marine biogenic factor reached a contribution of up to 50% in some samples. The most likely origin of the mixed combustion source is due to oil and gas extraction activities in Eastern Siberia. The two marine polymer gel sources predominantly occurred in autumn and winter. The small contribution of the marine gel sources at Mt. Zeppelin observatory in summer as opposed to regions closer to the North Pole is attributed to differences in ocean biology, vertical distribution of phytoplankton, and the earlier start of the summer season.http://dx.doi.org/10.1080/16000889.2019.1613143arctic aerosolssource apportionmentchemical analysismarine gelsice-related processes
collection DOAJ
language English
format Article
sources DOAJ
author Matthias Karl
Caroline Leck
Farshid Mashayekhy Rad
Are Bäcklund
Susana Lopez-Aparicio
Jost Heintzenberg
spellingShingle Matthias Karl
Caroline Leck
Farshid Mashayekhy Rad
Are Bäcklund
Susana Lopez-Aparicio
Jost Heintzenberg
New insights in sources of the sub-micrometre aerosol at Mt. Zeppelin observatory (Spitsbergen) in the year 2015
Tellus: Series B, Chemical and Physical Meteorology
arctic aerosols
source apportionment
chemical analysis
marine gels
ice-related processes
author_facet Matthias Karl
Caroline Leck
Farshid Mashayekhy Rad
Are Bäcklund
Susana Lopez-Aparicio
Jost Heintzenberg
author_sort Matthias Karl
title New insights in sources of the sub-micrometre aerosol at Mt. Zeppelin observatory (Spitsbergen) in the year 2015
title_short New insights in sources of the sub-micrometre aerosol at Mt. Zeppelin observatory (Spitsbergen) in the year 2015
title_full New insights in sources of the sub-micrometre aerosol at Mt. Zeppelin observatory (Spitsbergen) in the year 2015
title_fullStr New insights in sources of the sub-micrometre aerosol at Mt. Zeppelin observatory (Spitsbergen) in the year 2015
title_full_unstemmed New insights in sources of the sub-micrometre aerosol at Mt. Zeppelin observatory (Spitsbergen) in the year 2015
title_sort new insights in sources of the sub-micrometre aerosol at mt. zeppelin observatory (spitsbergen) in the year 2015
publisher Taylor & Francis Group
series Tellus: Series B, Chemical and Physical Meteorology
issn 1600-0889
publishDate 2019-01-01
description In order to evaluate the potential impact of the Arctic anthropogenic emission sources it is essential to understand better the natural aerosol sources of the inner Arctic and the atmospheric processing of the aerosols during their transport in the Arctic atmosphere. A 1-year time series of chemically specific measurements of the sub-micrometre aerosol during 2015 has been taken at the Mt. Zeppelin observatory in the European Arctic. A source apportionment study combined measured molecular tracers as source markers, positive matrix factorization, analysis of the potential source distribution and auxiliary information from satellite data and ground-based observations. The annual average sub-micrometre mass was apportioned to regional background secondary sulphate (56%), sea spray (17%), biomass burning (15%), secondary nitrate (5.8%), secondary marine biogenic (4.5%), mixed combustion (1.6%), and two types of marine gel sources (together 0.7%). Secondary nitrate aerosol mainly contributed towards the end of summer and during autumn. During spring and summer, the secondary marine biogenic factor reached a contribution of up to 50% in some samples. The most likely origin of the mixed combustion source is due to oil and gas extraction activities in Eastern Siberia. The two marine polymer gel sources predominantly occurred in autumn and winter. The small contribution of the marine gel sources at Mt. Zeppelin observatory in summer as opposed to regions closer to the North Pole is attributed to differences in ocean biology, vertical distribution of phytoplankton, and the earlier start of the summer season.
topic arctic aerosols
source apportionment
chemical analysis
marine gels
ice-related processes
url http://dx.doi.org/10.1080/16000889.2019.1613143
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