10 results on '"Nillius, Björn"'
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2. Preface: Special Issue on Probing the Open Ocean With the Research Sailing Yacht Eugen Seibold for Climate Geochemistry
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Schiebel, Ralf, Aardema, Hedy M., Calleja, Maria Ll., Dragoneas, Antonis, Heins, Lena, Hrabe de Angelis, Isabella, Pöhlker, Christopher, Slagter, Hans, Vonhof, Hubert, Walter, David, Arns, Anthea I., Adolphs, Nils, Auderset, Alexandra, Basic, Sanja, Bieler, Aaron, Brüwer, Jan D., Chaabane, Sonia, Cheng, Yafang, Chiliński, Michal T., Cybulski, Jonathan D., Disper, Thomas, Duprey, Nicolas, Eichele, Gregor, Fiedler, Björn, Fischer, Alexa, Foreman, Alan D., Fuchs, Bernhard M., Galer, Steve, Härri, Jana, Jochum, Klaus Peter, Jost, Adrian, Jung, Jonathan, Kleta, Henry, Lammel, Gerhard, Larink, Otto, Leibold, Patrick, Martínez‐García, Alfredo, Moretti, Simone, Müller, Jann‐Gerrit, Nillius, Björn, Pan, Xihao, Raj, Subha S., Repschläger, Janne, Rodrigues, Elizandro, Ruff, S. Emil, Schmitt, Mareike, Schmitter, Janine L., Lara, Andrew Sellers, Silva, Péricles, Smart, Sandi M., Sörgel, Matthias, Stoll, Brigitte, Su, Hang, Vogt, Meike, Wald, Tanja, Weber, Bettina, Weber, Jens, Weis, Ulrike, Amann, Rudolf, Arístegui, Javier, Dittmar, Thorsten, González, Melchor, O’Dea, Aaron, Pöschl, Ulrich, Haug, Gerald H., Schiebel, Ralf, Aardema, Hedy M., Calleja, Maria Ll., Dragoneas, Antonis, Heins, Lena, Hrabe de Angelis, Isabella, Pöhlker, Christopher, Slagter, Hans, Vonhof, Hubert, Walter, David, Arns, Anthea I., Adolphs, Nils, Auderset, Alexandra, Basic, Sanja, Bieler, Aaron, Brüwer, Jan D., Chaabane, Sonia, Cheng, Yafang, Chiliński, Michal T., Cybulski, Jonathan D., Disper, Thomas, Duprey, Nicolas, Eichele, Gregor, Fiedler, Björn, Fischer, Alexa, Foreman, Alan D., Fuchs, Bernhard M., Galer, Steve, Härri, Jana, Jochum, Klaus Peter, Jost, Adrian, Jung, Jonathan, Kleta, Henry, Lammel, Gerhard, Larink, Otto, Leibold, Patrick, Martínez‐García, Alfredo, Moretti, Simone, Müller, Jann‐Gerrit, Nillius, Björn, Pan, Xihao, Raj, Subha S., Repschläger, Janne, Rodrigues, Elizandro, Ruff, S. Emil, Schmitt, Mareike, Schmitter, Janine L., Lara, Andrew Sellers, Silva, Péricles, Smart, Sandi M., Sörgel, Matthias, Stoll, Brigitte, Su, Hang, Vogt, Meike, Wald, Tanja, Weber, Bettina, Weber, Jens, Weis, Ulrike, Amann, Rudolf, Arístegui, Javier, Dittmar, Thorsten, González, Melchor, O’Dea, Aaron, Pöschl, Ulrich, and Haug, Gerald H.
- Abstract
The 72‐foot sailing yacht Eugen Seibold is a new research platform for contamination‐free sampling of the water column and atmosphere for biological, chemical, and physical properties, and the exchange processes between the two realms. Ultimate goal of the project is a better understanding of the modern and past ocean and climate. Operations started in 2019 in the Northeast Atlantic, and will focus on the Tropical Eastern Pacific from 2023 until 2025. Laboratories for air and seawater analyses are equipped with down‐sized and automated state‐of‐the‐art technology for a comprehensive description of the marine carbon system including CO 2 concentration in the air and sea surface, pH, macro‐, and micro‐nutrient concentration (e.g., Fe, Cd), trace metals, and calcareous plankton. Air samples are obtained from ca. 13 m above sea surface and analyzed for particles (incl. black carbon and aerosols) and greenhouse gases. Plankton nets and seawater probes are deployed over the custom‐made A‐frame at the stern of the boat. Near Real‐Time Transfer of underway data via satellite connection allows dynamic expedition planning to maximize gain of information. Data and samples are analyzed in collaboration with the international expert research community. Quality controlled data are published for open access. The entire suite of data facilitates refined proxy calibration of paleoceanographic and paleoclimate archives at high temporal and spatial resolution in relation to seawater and atmospheric parameters. Plain Language Summary The new research sailing yacht Eugen Seibold ( ES ) enables clean, contamination‐free sampling of air and seawater to better understand the interactions between ocean and climate. For example, the oceans remove increasingly less carbon dioxide (CO 2 ) from the atmosphere the more saturated they are with CO 2 (ocean acidification). However, a detailed systematic understanding of air‐sea exchange processes remains to be developed. We analyze air and seawater
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- 2024
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3. ACRIDICON–CHUVA CAMPAIGN : Studying Tropical Deep Convective Clouds and Precipitation over Amazonia Using the New German Research Aircraft HALO
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Wendisch, Manfred, Pöschl, Ulrich, Andreae, Meinrat O., Machado, Luiz A. T., Albrecht, Rachel, Schlager, Hans, Rosenfeld, Daniel, Martin, Scot T., Abdelmonem, Ahmed, Afchine, Armin, Araùjo, Alessandro C., Artaxo, Paulo, Aufmhoff, Heinfried, Barbosa, Henrique M. J., Borrmann, Stephan, Braga, Ramon, Buchholz, Bernhard, Cecchini, Micael Amore, Costa, Anja, Curtius, Joachim, Dollner, Maximilian, Dorf, Marcel, Dreiling, Volker, Ebert, Volker, Ehrlich, André, Ewald, Florian, Fisch, Gilberto, Fix, Andreas, Frank, Fabian, Fütterer, Daniel, Heckl, Christopher, Heidelberg, Fabian, Hüneke, Tilman, Jäkel, Evelyn, Järvinen, Emma, Jurkat, Tina, Kanter, Sandra, Kästner, Udo, Kenntner, Mareike, Kesselmeier, Jürgen, Klimach, Thomas, Knecht, Matthias, Kohl, Rebecca, Kölling, Tobias, Krämer, Martina, Krüger, Mira, Krisna, Trismono Candra, Lavric, Jost V., Longo, Karla, Mahnke, Christoph, Manzi, Antonio O., Mayer, Bernhard, Mertes, Stephan, Minikin, Andreas, Molleker, Sergej, Münch, Steffen, Nillius, Björn, Pfeilsticker, Klaus, Pöhlker, Christopher, Roiger, Anke, Rose, Diana, Rosenow, Dagmar, Sauer, Daniel, Schnaiter, Martin, Schneider, Johannes, Schulz, Christiane, de Souza, Rodrigo A. F., Spanu, Antonio, Stock, Paul, Vila, Daniel, Voigt, Christiane, Walser, Adrian, Walter, David, Weigel, Ralf, Weinzierl, Bernadett, Werner, Frank, Yamasoe, Marcia A., Ziereis, Helmut, Zinner, Tobias, and Zöger, Martin
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- 2016
4. Preface: Special Issue on Probing the Open Ocean With the Research Sailing Yacht Eugen Seiboldfor Climate Geochemistry
- Author
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Schiebel, Ralf, Aardema, Hedy M., Calleja, Maria Ll., Dragoneas, Antonis, Heins, Lena, Hrabe de Angelis, Isabella, Pöhlker, Christopher, Slagter, Hans, Vonhof, Hubert, Walter, David, Arns, Anthea I., Adolphs, Nils, Auderset, Alexandra, Basic, Sanja, Bieler, Aaron, Brüwer, Jan D., Chaabane, Sonia, Cheng, Yafang, Chiliński, Michal T., Cybulski, Jonathan D., Disper, Thomas, Duprey, Nicolas, Eichele, Gregor, Fiedler, Björn, Fischer, Alexa, Foreman, Alan D., Fuchs, Bernhard M., Galer, Steve, Härri, Jana, Jochum, Klaus Peter, Jost, Adrian, Jung, Jonathan, Kleta, Henry, Lammel, Gerhard, Larink, Otto, Leibold, Patrick, Martínez‐García, Alfredo, Moretti, Simone, Müller, Jann‐Gerrit, Nillius, Björn, Pan, Xihao, Raj, Subha S., Repschläger, Janne, Rodrigues, Elizandro, Ruff, S. Emil, Schmitt, Mareike, Schmitter, Janine L., Lara, Andrew Sellers, Silva, Péricles, Smart, Sandi M., Sörgel, Matthias, Stoll, Brigitte, Su, Hang, Vogt, Meike, Wald, Tanja, Weber, Bettina, Weber, Jens, Weis, Ulrike, Amann, Rudolf, Arístegui, Javier, Dittmar, Thorsten, González, Melchor, O’Dea, Aaron, Pöschl, Ulrich, and Haug, Gerald H.
- Abstract
The 72‐foot sailing yacht Eugen Seiboldis a new research platform for contamination‐free sampling of the water column and atmosphere for biological, chemical, and physical properties, and the exchange processes between the two realms. Ultimate goal of the project is a better understanding of the modern and past ocean and climate. Operations started in 2019 in the Northeast Atlantic, and will focus on the Tropical Eastern Pacific from 2023 until 2025. Laboratories for air and seawater analyses are equipped with down‐sized and automated state‐of‐the‐art technology for a comprehensive description of the marine carbon system including CO2concentration in the air and sea surface, pH, macro‐, and micro‐nutrient concentration (e.g., Fe, Cd), trace metals, and calcareous plankton. Air samples are obtained from ca. 13 m above sea surface and analyzed for particles (incl. black carbon and aerosols) and greenhouse gases. Plankton nets and seawater probes are deployed over the custom‐made A‐frame at the stern of the boat. Near Real‐Time Transfer of underway data via satellite connection allows dynamic expedition planning to maximize gain of information. Data and samples are analyzed in collaboration with the international expert research community. Quality controlled data are published for open access. The entire suite of data facilitates refined proxy calibration of paleoceanographic and paleoclimate archives at high temporal and spatial resolution in relation to seawater and atmospheric parameters. The new research sailing yacht Eugen Seibold(ES) enables clean, contamination‐free sampling of air and seawater to better understand the interactions between ocean and climate. For example, the oceans remove increasingly less carbon dioxide (CO2) from the atmosphere the more saturated they are with CO2(ocean acidification). However, a detailed systematic understanding of air‐sea exchange processes remains to be developed. We analyze air and seawater as well as the exchange of greenhouse gases and other substances such as aerosols and soot (black carbon) between air and seawater at high resolution using modern materials and technologies. Scaled‐down, energy‐efficient, and automated probes developed over the past decade are being used to measure around 50 different characteristics of the marine environment. The work deck at the stern of the boat allows the use of custom‐made water samplers and plankton nets to study the ocean to below 1,000 m depth. In addition, the new data enables a better understanding of past ocean archives, such as the marine plankton accumulated in seafloor sediments, to reconstruct past climate changes. From 2019 to 2022, the S/Y ESsailed in the eastern North Atlantic and will operate in the tropical eastern Pacific until 2025. New research platform for contamination‐free sampling of the water column and atmosphere of biological, chemical, and physical propertiesComprehensive marine geochemical analyzes including carbon (e.g., CO2) in air and sea surfaceProxy calibration of paleoclimate archives at high temporal and spatial resolution in relation to seawater and atmospheric parameters New research platform for contamination‐free sampling of the water column and atmosphere of biological, chemical, and physical properties Comprehensive marine geochemical analyzes including carbon (e.g., CO2) in air and sea surface Proxy calibration of paleoclimate archives at high temporal and spatial resolution in relation to seawater and atmospheric parameters
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- 2024
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5. A comprehensive laboratory study on the immersion freezing behavior of illite NX particles : a comparison of 17 ice nucleation measurement techniques
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Hiranuma, Naruki, Augustin-Bauditz, Stefanie, Bingemer, Heinz, Budke, Carsten, Curtius, Joachim, Danielczok, Anja, Diehl, Karoline, Dreischmeier, Katharina, Ebert, Martin, Frank, Fabian, Hoffmann, Nadine, Kandler, Konrad, Kiselev, Alexei, Koop, Thomas, Leisner, Thomas, Möhler, Ottmar, Nillius, Björn, Peckhaus, Andreas, Rose, Diana, Hader, John D., Hill, Thomas C., Kanji, Zamin A., Kulkarni, Gargi, Levin, Ezra J. T., McCluskey, Christina S., Murakami, Masataka, Murray, Benjamin J., Niedermeier, Dennis, Petters, Markus D., O'Sullivan, Daniel, Saito, Atsushi, Schill, Gregory P., Tajiri, Takuya, Tolbert, Margret A., Welti, André, Whale, Thomas F., Wright, Timothy P., and Yamashita, Katsuya
- Subjects
ddc:550 - Abstract
Immersion freezing is the most relevant heterogeneous ice nucleation mechanism through which ice crystals are formed in mixed-phase clouds. In recent years, an increasing number of laboratory experiments utilizing a variety of instruments have examined immersion freezing activity of atmospherically relevant ice-nucleating particles. However, an intercomparison of these laboratory results is a difficult task because investigators have used different ice nucleation (IN) measurement methods to produce these results. A remaining challenge is to explore the sensitivity and accuracy of these techniques and to understand how the IN results are potentially influenced or biased by experimental parameters associated with these techniques. Within the framework of INUIT (Ice Nuclei Research Unit), we distributed an illite-rich sample (illite NX) as a representative surrogate for atmospheric mineral dust particles to investigators to perform immersion freezing experiments using different IN measurement methods and to obtain IN data as a function of particle concentration, temperature (T), cooling rate and nucleation time. A total of 17 measurement methods were involved in the data intercomparison. Experiments with seven instruments started with the test sample pre-suspended in water before cooling, while 10 other instruments employed water vapor condensation onto dry-dispersed particles followed by immersion freezing. The resulting comprehensive immersion freezing data set was evaluated using the ice nucleation active surface-site density, ns, to develop a representative ns(T) spectrum that spans a wide temperature range (−37 °C < T < −11 °C) and covers 9 orders of magnitude in ns. In general, the 17 immersion freezing measurement techniques deviate, within a range of about 8 °C in terms of temperature, by 3 orders of magnitude with respect to ns. In addition, we show evidence that the immersion freezing efficiency expressed in ns of illite NX particles is relatively independent of droplet size, particle mass in suspension, particle size and cooling rate during freezing. A strong temperature dependence and weak time and size dependence of the immersion freezing efficiency of illite-rich clay mineral particles enabled the ns parameterization solely as a function of temperature. We also characterized the ns(T) spectra and identified a section with a steep slope between −20 and −27 °C, where a large fraction of active sites of our test dust may trigger immersion freezing. This slope was followed by a region with a gentler slope at temperatures below −27 °C. While the agreement between different instruments was reasonable below ~ −27 °C, there seemed to be a different trend in the temperature-dependent ice nucleation activity from the suspension and dry-dispersed particle measurements for this mineral dust, in particular at higher temperatures. For instance, the ice nucleation activity expressed in ns was smaller for the average of the wet suspended samples and higher for the average of the dry-dispersed aerosol samples between about −27 and −18 °C. Only instruments making measurements with wet suspended samples were able to measure ice nucleation above −18 °C. A possible explanation for the deviation between −27 and −18 °C is discussed. Multiple exponential distribution fits in both linear and log space for both specific surface area-based ns(T) and geometric surface area-based ns(T) are provided. These new fits, constrained by using identical reference samples, will help to compare IN measurement methods that are not included in the present study and IN data from future IN instruments.
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- 2015
6. Intercomparing different devices for the investigation of ice nucleating particles using Snomax as test substance
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Wex, Heike, Augustin-Bauditz, Stefanie, Boose, Yvonne, Budke, Carsten, Curtius, Joachim, Diehl, Karoline, Dreyer, Axel, Frank, Fabian, Hartmann, Susan, Hiranuma, Naruki, Jantsch, Evelyn, Kanji, Zamin A., Kiselev, Alexei, Koop, Thomas, Möhler, Ottmar, Niedermeier, Dennis, Nillius, Björn, Rösch, Michael, Rose, Diana, Schmidt, C., Steinke, Isabelle, and Stratmann, Frank
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Earth sciences ,ddc:550 - Abstract
Seven different instruments and measurement methods were used to examine the immersion freezing of bacterial ice nuclei from Snomax® (hereafter Snomax), a product containing ice-active protein complexes from non-viable Pseudomonas syringae bacteria. The experimental conditions were kept as similar as possible for the different measurements. Of the participating instruments, some examined droplets which had been made from suspensions directly, and the others examined droplets activated on previously generated Snomax particles, with particle diameters of mostly a few hundred nanometers and up to a few micrometers in some cases. Data were obtained in the temperature range from −2 to −38 °C, and it was found that all ice-active protein complexes were already activated above −12 °C. Droplets with different Snomax mass concentrations covering 10 orders of magnitude were examined. Some instruments had very short ice nucleation times down to below 1 s, while others had comparably slow cooling rates around 1 K min−1. Displaying data from the different instruments in terms of numbers of ice-active protein complexes per dry mass of Snomax, nm, showed that within their uncertainty, the data agree well with each other as well as to previously reported literature results. Two parameterizations were taken from literature for a direct comparison to our results, and these were a time-dependent approach based on a contact angle distribution (Niedermeier et al., 2014) and a modification of the parameterization presented in Hartmann et al. (2013) representing a time-independent approach. The agreement between these and the measured data were good; i.e., they agreed within a temperature range of 0.6 K or equivalently a range in nm of a factor of 2. From the results presented herein, we propose that Snomax, at least when carefully shared and prepared, is a suitable material to test and compare different instruments for their accuracy of measuring immersion freezing.
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- 2015
- Full Text
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7. Single-particle characterization of ice-nucleating particles and iceparticles residuals sampled by three different techniques
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Kandler, Konrad, Worringen, Annette, Schmitz, Josef, Rose, Diana, Curtius, Joachim, Kupiszewski, Piotr, Weingartner, Ernest, Vochezer, Paul, Schneider, Johannes, Schmidt, Susan, Weinbruch, Stephan, Ebert, Martin, Benker, Nathalie, Dirsch, Thomas, Mertes, Stephan, Schenk, Ludwig, Kästner, Udo, Frank, Fabian, Nillius, Björn, and Bundke, Ulrich
- Subjects
ddc:550 - Published
- 2015
8. Intercomparing different devices for the investigation of ice nucleating particles using Snomax (R) as test substance
- Author
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Wex, Heike, Augustin-Bauditz, Stefanie, Boose, Yvonne, Budke, Carsten, Curtius, Joachim, Diehl, Karoline, Dreyer, Axel, Frank, F., Hartmann, Susan, Hiranuma, Naruki, Jantsch, E., Kanji, Zamin A, Kiselev, Alexei A., Koop, Thomas, Möhler, Ottmar, Niedermeier, Dennis, Nillius, Björn, Rosch, M., Rose, Diana, Schmidt, C., Steinke, Isabelle, and Stratmann, Frank
- Abstract
Seven different instruments and measurement methods were used to examine the immersion freezing of bacterial ice nuclei from Snomax® (hereafter Snomax), a product containing ice-active protein complexes from non-viable Pseudomonas syringae bacteria. The experimental conditions were kept as similar as possible for the different measurements. Of the participating instruments, some examined droplets which had been made from suspensions directly, and the others examined droplets activated on previously generated Snomax particles, with particle diameters of mostly a few hundred nanometers and up to a few micrometers in some cases. Data were obtained in the temperature range from −2 to −38 °C, and it was found that all ice-active protein complexes were already activated above −12 °C. Droplets with different Snomax mass concentrations covering 10 orders of magnitude were examined. Some instruments had very short ice nucleation times down to below 1 s, while others had comparably slow cooling rates around 1 K min−1. Displaying data from the different instruments in terms of numbers of ice-active protein complexes per dry mass of Snomax, nm, showed that within their uncertainty, the data agree well with each other as well as to previously reported literature results. Two parameterizations were taken from literature for a direct comparison to our results, and these were a time-dependent approach based on a contact angle distribution (Niedermeier et al., 2014) and a modification of the parameterization presented in Hartmann et al. (2013) representing a time-independent approach. The agreement between these and the measured data were good; i.e., they agreed within a temperature range of 0.6 K or equivalently a range in nm of a factor of 2. From the results presented herein, we propose that Snomax, at least when carefully shared and prepared, is a suitable material to test and compare different instruments for their accuracy of measuring immersion freezing., Atmospheric Chemistry and Physics, 15 (3), ISSN:1680-7375, ISSN:1680-7367
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- 2015
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9. A broad supersaturation scanning (BS2) approach for rapid measurement of aerosol particle hygroscopicity and cloud condensation nuclei activity
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Su, Hang, primary, Cheng, Yafang, additional, Ma, Nan, additional, Wang, Zhibin, additional, Wang, Xiaoxiang, additional, Pöhlker, Mira L., additional, Nillius, Björn, additional, Wiedensohler, Alfred, additional, and Pöschl, Ulrich, additional
- Published
- 2016
- Full Text
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10. Single-particle characterization of ice-nucleating particles and ice particles residuals sampled by three different techniques
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EGU General Assembly 2015, Kandler, Konrad, Worringen, Annette, Benker, Nathalie, Dirsch, Thomas, Mertes, Stephan, Schenk, Ludwig, Kästner, Udo, Frank, Fabian, Nillius, Björn, Bundke, Ulrich, Rose, Diana, Curtius, Joachim, Kupiszewski, Piotr, Weingartner, Ernest, Vochezer, Paul, Schneider, Johannes, Schmidt, Susan, Weinbruch, Stephan, Ebert, Martin, EGU General Assembly 2015, Kandler, Konrad, Worringen, Annette, Benker, Nathalie, Dirsch, Thomas, Mertes, Stephan, Schenk, Ludwig, Kästner, Udo, Frank, Fabian, Nillius, Björn, Bundke, Ulrich, Rose, Diana, Curtius, Joachim, Kupiszewski, Piotr, Weingartner, Ernest, Vochezer, Paul, Schneider, Johannes, Schmidt, Susan, Weinbruch, Stephan, and Ebert, Martin
- Abstract
During January/February 2013, at the High Alpine Research Station Jungfraujoch a measurement campaign was carried out, which was centered on atmospheric ice-nucleating particles (INP) and ice particle residuals (IPR). Three different techniques for separation of INP and IPR from the non-ice-active particles are compared. The Ice Selective Inlet (ISI) and the Ice Counterflow Virtual Impactor (Ice-CVI) sample ice particles from mixed phase clouds and allow for the analysis of the residuals. The combination of the Fast Ice Nucleus Chamber (FINCH) and the Ice Nuclei Pumped Counterflow Virtual Impactor (IN-PCVI) provides ice-activating conditions to aerosol particles and extracts the activated INP for analysis.Collected particles were analyzed by scanning electron microscopy and energy-dispersive X-ray microanalysis to determine size, chemical composition and mixing state. All INP/IPR-separating techniques had considerable abundances (median 20 – 70 %) of instrumental contamination artifacts (ISI: Si-O spheres, probably calibration aerosol; Ice-CVI: Al-O particles; FINCH+IN-PCVI: steel particles). Also, potential sampling artifacts (e.g., pure soluble material) occurred with a median abundance of < 20 %. While these could be explained as IPR by ice break-up, for INP their IN-ability pathway is less clear. After removal of the contamination artifacts, silicates and Ca-rich particles, carbonaceous material and metal oxides were the major INP/IPR particle types separated by all three techniques. Soot was a minor contributor. Lead was detected in less than 10 % of the particles, of which the majority were internal mixtures with other particle types. Sea-salt and sulfates were identified by all three methods as INP/IPR. Most samples showed a maximum of the INP/IPR size distribution at 400 nm geometric diameter. In a few cases, a second super-micron maximum was identified. Soot/carbonaceous material and metal oxides were present mainly in the submicron range. ISI and FINCH yie
- Published
- 2015
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