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Author |
Artaxo, P.; Storms, H.; Bruynseels, F.; Van Grieken, R.; Maenhaut, W. |
![find record details (via OpenURL) openurl](img/xref.gif)
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Title |
Composition and sources of aerosols from the Amazon basin |
Type |
A1 Journal article |
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Year |
1988 |
Publication |
Journal of geophysical research |
Abbreviated Journal |
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Volume |
93 |
Issue ![sorted by Issue field, descending order (down)](img/sort_desc.gif) |
D2 |
Pages |
1605-1615 |
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Keywords |
A1 Journal article; AXES (Antwerp X-ray Analysis, Electrochemistry and Speciation) |
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Abstract |
Aerosols were sampled in the Amazon Basin, as part of the Global Tropospheric Experiment (GTE), during the Amazon Boundary Layer Experiment (ABLE 2A) in JulyAugust 1985. Fine- and coarse-particle fractions were analyzed for 22 elements by particle-induced X ray emission. Gravimetric mass, black carbon, sulfate, and nitrate concentrations were also determined. Morphological and trace element measurements of individual particles were carried out by automated electron probe X ray microanalysis. Various receptor models, including multivariate methods and a chemical mass balance model, were employed in the interpretation of the bulk trace element concentrations. Three factors explained over 85% of the variability of fine- and coarse-mode variables. On the basis of the elemental composition of the factors, two could be identified as plant related, and the third was a soil dust component. Of the coarse-mode aerosol mass concentration (of 7.6±1.6 μg/m3), 62% could be attributed to aerosols released by the vegetation and 11% to soil dust. In the fine mode, soil dust accounted for less than 10% of the measured mass concentration (of 6.8±3.9 μg/m3). The variables related to the plant component were K, P, S, Ca, Mg, Cl, Rb, and the gravimetric mass. The elemental profile of the plant component resembled the bulk plant composition. By single-particle analysis coupled with hierarchical cluster analysis, six to nine different biogenic-related particle groups could be identified in the fine- and coarse-aerosol modes. Almost all particle types consisted predominantly of carbonaceous material, with trace amounts of K, S, Ca, P, Cl, and Na. Only one group, comprising less than 11% of the total number of particles, consisted of soil dustrelated aerosol. |
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A1988M303000024 |
Publication Date |
2008-02-06 |
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0148-0227; 2156-2202; 0022-1406; 0196-6928; 0196-6936; 0885-3401; 8755-8556; 0196-2256; 0747-7309; 1 |
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UA library record; WoS full record; WoS citing articles |
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Call Number |
UA @ admin @ c:irua:113609 |
Serial |
7702 |
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Author |
Graham, B.; Guyon, P.; Maenhaut, W.; Taylor, P.E.; Ebert, M.; Matthias-Maser, S.; Mayol-Bracero, O.L.; Godoi, R.H.M.; Artaxo, P.; Meixner, F.X.; Lima Moura, M.A.; d'Almeida Rocha, C.H.E.; Van Grieken, R.; Glovsky, M.M.; Flagan, R.C.; Andreae, M.O. |
![find record details (via OpenURL) openurl](img/xref.gif)
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Title |
Composition and diurnal variability of the natural Amazonian aerosol |
Type |
A1 Journal article |
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Year |
2003 |
Publication |
Journal of geophysical research |
Abbreviated Journal |
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Volume |
24 |
Issue ![sorted by Issue field, descending order (down)](img/sort_desc.gif) |
4765 |
Pages |
5,1-16 |
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Keywords |
A1 Journal article; AXES (Antwerp X-ray Analysis, Electrochemistry and Speciation) |
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000187858400009 |
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2003-12-17 |
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0148-0227; 2156-2202; 0022-1406; 0196-6928; 0196-6936; 0885-3401; 8755-8556; 0196-2256; 0747-7309; 1 |
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UA @ admin @ c:irua:43523 |
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7700 |
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Arana, A.; Loureiro, A.L.; Barbosa, H.M.J.; Van Grieken, R.; Artaxo, P. |
![goto web page (via DOI) doi](http://nano.uantwerpen.be/nanorefs/img/doi.gif)
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Title |
Optimized energy dispersive X-ray fluorescence analysis of atmospheric aerosols collected at pristine and perturbed Amazon Basin sites |
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A1 Journal article |
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Year |
2014 |
Publication |
X-ray spectrometry |
Abbreviated Journal |
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Volume |
43 |
Issue ![sorted by Issue field, descending order (down)](img/sort_desc.gif) |
4 |
Pages |
228-237 |
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Keywords |
A1 Journal article; AXES (Antwerp X-ray Analysis, Electrochemistry and Speciation) |
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Abstract |
Elemental composition of aerosols is important to source apportionment studies and to understand atmospheric processes that influence aerosol composition. Energy dispersive X-ray fluorescence spectroscopy was applied for measuring the elemental composition of Amazonian atmospheric aerosols. The instrument used was a spectrometer Epsilon 5, PANalytical B. V., with tridimensional geometry that reduces the background signal with a polarized X-ray detection. The measurement conditions were optimized for low-Z elements, e. g. Mg, Al, Si, that are present at very low concentrations in the Amazon. From Na to K, our detection limits are about 50% to 75% lower than previously published results for similar instrument. Calibration was performed using Micromatter standards, except for P whose standard was produced by nebulization of an aqueous solution of KH2PO4 at our laboratory. The multi-element reference material National Institute of Standards and Technology-2783 (air particulate filter) was used for evaluating the accuracy of the calibration procedure of the 22 elements in our standard analysis routine, and the uncertainty associated with calibration procedures was evaluated. The overall performance of the instrument and validation of our measurements were assessed by comparison with results obtained from parallel analysis using particle-induced X-ray emission and another Epsilon 5 spectrometer. The elemental composition in 660 samples collected at a pristine site in the Amazon Basin and of 1416 samples collected at a site perturbed by land use change was determined. Our measurements show trace elements associated with biogenic aerosols, soil dust, biomass burning, and sea-salt, even for the very low concentrations as observed in Amazonia. Copyright (C) 2014 John Wiley & Sons, Ltd. |
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000337724600006 |
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2014-06-09 |
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0049-8246 |
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UA library record; WoS full record; WoS citing articles |
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no |
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Call Number |
UA @ admin @ c:irua:118419 |
Serial |
8342 |
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Author |
Wouters, L.; Artaxo, P.; Van Grieken, R. |
![find record details (via OpenURL) openurl](img/xref.gif)
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Title |
Laser microprobe mass analysis of individual Antarctic aerosol particles |
Type |
A1 Journal article |
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Year |
1990 |
Publication |
International journal of environmental analytical chemistry |
Abbreviated Journal |
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Volume |
38 |
Issue ![sorted by Issue field, descending order (down)](img/sort_desc.gif) |
3 |
Pages |
427-438 |
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Keywords |
A1 Journal article; AXES (Antwerp X-ray Analysis, Electrochemistry and Speciation) |
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Abstract |
Individual Antarctic aerosol particles in the 0.54 μm aerodynamic diameter range were analyzed using laser microprobe mass analysis (LAMMA). As they were sampled near the ocean, the great majority consists of seasalt, transformed to various degrees in the atmosphere. Major alterations include the association of an excess sulfate and methane sulfonate with these particles. Sulfate-rich particles containing little or no chloride were found mostly in the smallest size fraction (0.51 μm), where they account for some 5% of all particles: they are most likely highly transformed seasalt. Aluminosilicates, on the other hand, only appear among the coarser particles: they represent 2% of the particulates in the 24 μm range. The remainder of the aerosol consists of organic, Fe-rich, K-rich and Zn-rich particles. The latter groups have very low abundances: always less than 1% of the population of the impactor stage(s) onto which they were collected. |
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A1990CN56100011 |
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2007-07-07 |
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0306-7319 |
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UA library record; WoS full record; WoS citing articles |
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Call Number |
UA @ admin @ c:irua:116580 |
Serial |
8160 |
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Author |
Rojas, C.M.; Artaxo, P.; Van Grieken, R. |
![goto web page (via DOI) doi](http://nano.uantwerpen.be/nanorefs/img/doi.gif)
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Title |
Aerosols in Santiago de Chile : a study using receptor modeling with X-ray fluorescence and single particle analysis |
Type |
A1 Journal article |
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Year |
1990 |
Publication |
Atmospheric environment: part B : urban atmosphere |
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Volume |
24 |
Issue ![sorted by Issue field, descending order (down)](img/sort_desc.gif) |
2 |
Pages |
227-241 |
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Keywords |
A1 Journal article; AXES (Antwerp X-ray Analysis, Electrochemistry and Speciation) |
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Abstract |
Between 15 January and 26 February 1987, 51 fine and coarse mode aerosol samples were collected at the Universidad de Santiago de Chile Planetarium using a dichotomous sampler. The samples were analyzed by X-ray fluorescence for up to 17 elements (Mg, Al, Si, P, S, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, Br and Pb). Aerosol particles were individually studied by Electron Probe Microanalysis (EPMA) and Laser Microprobe Mass Analysis (LAMMA). The data set consisting of aerosol elemental concentrations and meteorological variables was subjected to Principal Factor Analysis (PFA), allowing the identification of six fine mode particle source classes (soil, industrial, sulfate particles, traffic, residual oil, wood-burnings), and five coarse mode particle source classes (soil, industrial, traffic, residual oil, sulfate particles). Both PFA solutions explained about 81 and 90% of the total variance in the data set, respectively. The regression of elemental mass concentrations on the Absolute Principal Factor Scores allowed the estimation of the contribution of the different source classes to the Santiago aerosol. Within the fine fraction, secondary SO42− particles were responsible for about 49% of the fine mode aerosol mass concentration, while 26, 13, 6.4 and 5.6% were attributed to wood-burning/car exhausts, residual oil combustion, soil dust/metallurgical, and soil dust/wood-burning releases, respectively. The coarse fraction source apportionment was mainly dominated by soil dust, accounting for 74% of the coarse mode aerosol mass concentration. A composite of soil dust and industrial release accounted for 13%; a composite of secondary sulfates contributed with 9%; a composite of soil dust and automotive emissions, and secondary sulfates were responsible for 4 and 0.03% of the coarse aerosol mass concentration, respectively. EPMA results are in satisfactory agreement with those from the bulk analysis and allowed the identification of eight particle types in both fine and coarse mode aerosols, pertaining to different source classes, namely soil, seaspray, secondary SO42−, metallurgical emissions and biomass burning release. EPMA also evidenced that one of the most abundant particle types corresponded to marine aerosol, having an average diameter of 0.7 μm for the fine mode and 2.2 μm for the coarse mode aerosol. LAMMA results indicate that, in fact, seaspray has been transported into the city of Santiago de Chile airshed, suffering several transformations and a sulfur enrichment. This analytical technique also provided evidence of the abundance of carbon-rich particles, which were not detected by either the bulk X-ray analysis or EPMA; they are probably due to fossil-fuel combustion releases. |
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2003-08-06 |
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0957-1272; 1878-2132 |
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Call Number |
UA @ admin @ c:irua:116456 |
Serial |
7427 |
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Permanent link to this record |
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Author |
Artaxo, P.; Maenhaut, W.; Storms, H.; Van Grieken, R. |
![find record details (via OpenURL) openurl](img/xref.gif)
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Title |
Aerosol characteristics and sources for the Amazon Basin during the wet season |
Type |
A1 Journal article |
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Year |
1990 |
Publication |
Journal of geophysical research |
Abbreviated Journal |
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Volume |
95 |
Issue ![sorted by Issue field, descending order (down)](img/sort_desc.gif) |
10 |
Pages |
16971-16985 |
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Keywords |
A1 Journal article; AXES (Antwerp X-ray Analysis, Electrochemistry and Speciation) |
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Abstract |
As a part of the NASA Global Tropospheric Experiment (GTE), aerosols were sampled in the tropical rain forest of the Amazon Basin during the Amazon Boundary Layer Experiment (ABLE 2B) in April and May 1987, in the wet season, when no forest burning occurs. Fine (dp < 2.0 μm) and coarse (2.0 < dp < 15 μm) aerosol fractions were collected using stacked filter units, at three sites under the forest canopy and at three levels of a tower inside the jungle. Particle-induced X ray emission (PIXE) was used to measure concentrations of 22 elements (Na, Mg, Al, Si, P, S, Cl, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, Br, Rb, Sr, Zr, and Pb). Morphological and trace element measurements of individual particles were carried out by automated electron probe X ray microanalysis. Gravimetric analysis was performed to obtain the fine and coarse aerosol mass concentration. Absolute factor analysis was used to interpret the large data set of the trace element concentrations and to obtain elemental source profiles. Hierarchical cluster analysis was used to derive groups of individual particles. The concentrations of soil dust related elements (Al, Si, Ti, Fe, Mn) were 5 times larger in the wet season compared to the 1985 ABLE 2A dry season experiment. Biogenic aerosol related elements in the fine fraction showed lower concentrations in the wet season. Fine aerosol mass concentration averaged only 2.1±0.7 μg m−3, while the average coarse mass concentration was 6.1±1.8 μg m −3. Sulphur concentrations averaged 76±14 ng m −3 in the fine fraction and 37±9 ng m −3 in the coarse fraction. Biogenic aerosol-related elements were dominant under the forest canopy, while soil dust dominated at the top of the forest canopy. Only two factors explained about 90% of the data variability for the fine and coarse aerosol fractions. These were soil dust (represented mainly by Al, Si, Ti, Mn, and Fe) and biogenic aerosol (represented by K, P, Cl, S, Zn, and the aerosol mass concentration). Source profiles showed a homogeneous aerosol distribution with similar elemental compositions at the different sampling sites. Enrichment factor calculations revealed a soil dust elemental profile similar to the average bulk soil composition, and a biogenic component similar to the plant bulk elemental composition. Total aerosol mass source apportionment showed that biogenic particles account for 5595% of the airborne concentrations. The analysis of individual aerosol particles showed that the biogenic particles consist of leaf fragments, pollen grains, fungi, algae, and other types of particles. Several groups of particles with K, Cl, P, S, and Ca as minor elements could easily be identified as biogenic particles on the basis of their morphology. Considering the vast area of tropical rain forests and the concentrations measured in this work, it is possible that biogenic particles can play an important role in the global aerosol budget and in the global biogeochemical cycles of various elements. |
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A1990EB20200051 |
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2008-02-06 |
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0148-0227; 2156-2202; 0022-1406; 0196-6928; 0196-6936; 0885-3401; 8755-8556; 0196-2256; 0747-7309; 1 |
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UA library record; WoS full record; WoS citing articles |
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Call Number |
UA @ admin @ c:irua:116931 |
Serial |
7422 |
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Author |
Van Grieken, R.; Artaxo, P.; Xhoffer, C. |
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Title |
Automated EPXMA of individual environmental particles |
Type |
P3 Proceeding |
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Year |
1992 |
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P3 Proceeding; AXES (Antwerp X-ray Analysis, Electrochemistry and Speciation) |
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UA @ admin @ c:irua:2860 |
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7537 |
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Author |
Xhoffer, C.; Wouters, L.; Artaxo, P.; van Put, A.; Van Grieken, R. |
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Title |
Characterization of individual environmental particles by beam techniques |
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H3 Book chapter |
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Year |
1992 |
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107-143
T2 - Environmental particles, volume 1 / B |
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Keywords |
H3 Book chapter; AXES (Antwerp X-ray Analysis, Electrochemistry and Speciation) |
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UA @ admin @ c:irua:2853 |
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7623 |
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Storms, H.; Artaxo, P.; Bruynseels, F.; Van Grieken, R. |
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Title |
Individual particle analysis by automated EPMA for the improvement of source apportionment for remote aerosols |
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H3 Book chapter |
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1987 |
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Abbreviated Journal |
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343-345
T2 - Microbeam analysis 1987 / Geiss, R.H. |
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H3 Book chapter; AXES (Antwerp X-ray Analysis, Electrochemistry and Speciation) |
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UA @ admin @ c:irua:117525 |
Serial |
8077 |
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Author |
Bruynseels, F.; Artaxo, P.; Storms, H.; Van Grieken, R. |
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Title |
LAMMA-study of aerosol samples collected in the Amazon basin |
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H3 Book chapter |
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1987 |
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355-358
T2 - Microbeam analysis 1987 / Geiss, R.H. |
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H3 Book chapter; AXES (Antwerp X-ray Analysis, Electrochemistry and Speciation) |
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Call Number |
UA @ admin @ c:irua:117527 |
Serial |
8151 |
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Author |
Van Grieken, R.; Artaxo, P.; Bernard, P.; Leysen, L.; Otten, P.; Storms, H.; Van Put, A.; Wouters, L.; Xhoffer, C. |
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Title |
Micro-analysis of individual environmental particles |
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A1 Journal article |
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Year |
1990 |
Publication |
Chemia analityczna |
Abbreviated Journal |
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Volume |
35 |
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75-89 |
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A1 Journal article; AXES (Antwerp X-ray Analysis, Electrochemistry and Speciation) |
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A1990FG37600010 |
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0009-2223 |
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Additional Links |
UA library record; WoS full record; WoS citing articles |
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Times cited |
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Open Access |
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Approved |
no |
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Call Number |
UA @ admin @ c:irua:116932 |
Serial |
8227 |
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Permanent link to this record |
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Author |
Artaxo, P.; Van Grieken, R.; Watt, F.; Jaksic, M. |
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Title |
The microanalysis of individual atmospheric aerosol particles by electron, proton and laser microprobe |
Type |
P3 Proceeding |
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Year |
1990 |
Publication |
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Abbreviated Journal |
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Issue ![sorted by Issue field, descending order (down)](img/sort_desc.gif) |
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Keywords |
P3 Proceeding; AXES (Antwerp X-ray Analysis, Electrochemistry and Speciation) |
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Wos |
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Edition |
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ISSN |
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ISBN |
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Additional Links |
UA library record |
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Impact Factor |
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Times cited |
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Open Access |
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Notes |
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Approved |
no |
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Call Number |
UA @ admin @ c:irua:117515 |
Serial |
8235 |
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Permanent link to this record |
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Author |
Artaxo, P.; Rabello, M.L.C.; Maenhaut, W.; Van Grieken, R. |
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Title |
Trace elements and individual particle analysis of atmospheric aerosols from the Antarctic peninsula |
Type |
A3 Journal article |
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Year |
1992 |
Publication |
Tellus |
Abbreviated Journal |
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Volume |
44b |
Issue ![sorted by Issue field, descending order (down)](img/sort_desc.gif) |
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Pages |
318-334 |
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Keywords |
A3 Journal article; AXES (Antwerp X-ray Analysis, Electrochemistry and Speciation) |
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Abstract |
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Corporate Author |
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Thesis |
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Publisher |
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Place of Publication |
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Editor |
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Wos |
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Publication Date |
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Abbreviated Series Title |
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Series Volume |
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Series Issue |
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Edition |
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ISBN |
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Additional Links |
UA library record |
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Impact Factor |
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Times cited |
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Open Access |
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Notes |
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Approved |
no |
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Call Number |
UA @ admin @ c:irua:2845 |
Serial |
8689 |
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Permanent link to this record |