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  5. Composition and mixing state of atmospheric aerosols determined by electron microscopy: method development and application to aged Saharan dust deposition in the Caribbean boundary layer
 
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2018
Zweitveröffentlichung
Artikel
Verlagsversion

Composition and mixing state of atmospheric aerosols determined by electron microscopy: method development and application to aged Saharan dust deposition in the Caribbean boundary layer

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TUDa URI
tuda/4914
URN
urn:nbn:de:tuda-tuprints-113829
DOI
10.25534/tuprints-00011382
Autor:innen
Kandler, Konrad
Schneiders, Kilian
Ebert, Martin
Hartmann, Markus
Weinbruch, Stephan
Prass, Maria
Pöhlker, Christopher
Kurzbeschreibung (Abstract)

The microphysical properties, composition and mixing state of mineral dust, sea salt and secondary compounds were measured by active and passive aerosol sampling, followed by electron microscopy and X-ray fluorescence in the Caribbean marine boundary layer. Measurements were carried out at Ragged Point, Barbados during June–July 2013 and August 2016. Techniques are presented and evaluated, which allow for statements on atmospheric aerosol concentrations and aerosol mixing state based on collected samples. It became obvious that in the diameter range with the highest dust deposition the deposition velocity models disagree by more than 2 orders of magnitude. Aerosol at Ragged Point was dominated by dust, sea salt and soluble sulfates in varying proportions. The contribution of sea salt was dependent on local wind speed. Sulfate concentrations were linked to long-range transport from Africa and Europe, and South America and the southern Atlantic Ocean. Dust sources were located in western Africa. The dust silicate composition was not significantly varied. Pure feldspar grains were 3 % of the silicate particles, of which about a third were K-feldspar. The average dust deposition observed was 10 mg m−2 d−1 (range of 0.5–47 mg m−2 d−1), of which 0.67 mg m−2 d−1 was iron and 0.001 mg m−2 d−1 phosphorus. Iron deposition was mainly driven by silicate particles from Africa. Dust particles were mixed internally to a minor fraction (10 %), mostly with sea salt and less frequently with sulfate. It was estimated that the average dust deposition velocity under ambient conditions is increased by the internal mixture by 30 % – 140 % for particles between 1 and 10 µm dust aerodynamic diameter, with approximately 35 % at the mass median diameter of deposition (7.0 µm). For this size, an effective deposition velocity of 6.4 mm s−1 (geometric standard deviation of 3.1 over all individual particles) was observed.

Sprache
Englisch
Fachbereich/-gebiet
11 Fachbereich Material- und Geowissenschaften > Geowissenschaften
DDC
500 Naturwissenschaften und Mathematik > 550 Geowissenschaften
Institution
Universitäts- und Landesbibliothek Darmstadt
Ort
Darmstadt
Titel der Zeitschrift / Schriftenreihe
Atmospheric Chemistry and Physics
Startseite
13429
Endseite
13455
Jahrgang der Zeitschrift
18
Heftnummer der Zeitschrift
18
ISSN
1680-7324
Verlag
Copernicus
Publikationsjahr der Erstveröffentlichung
2018
Verlags-DOI
10.5194/acp-18-13429-2018
PPN
457915927
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Notice on corrigendum
The requested paper has a corresponding corrigendum published. Please read the corrigendum first before downloading the article.

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